| OMIM ID |
Human Disease |
| 613652 |
C1q Deficiency; C1QD |
| 615082 |
C3hex, Ability to Smell |
| 114030 |
Cafe-Au-Lait Spots, Multiple |
| 114000 |
Caffey Disease |
| 211770 |
Cahmr Syndrome |
| 114065 |
Calcific Aortic Disease with Immunologic Abnormalities, Familial |
| 211800 |
Calcification of Joints and Arteries; CALJA |
| 601199 |
Calcium-Sensing Receptor; CASR |
| 114140 |
Callosities, Hereditary Painful |
| 302030 |
Calvarial Hyperostosis |
| 604257 |
Camera-Marugo-Cohen Syndrome |
| 211890 |
Campomelia, Cumming Type |
| 114290 |
Campomelic Dysplasia (7 mouse models) |
| 114150 |
Camptobrachydactyly |
| 114200 |
Camptodactyly 1; CAMPD1 |
| 208250 |
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome; CACP (1 mouse model) |
| 211965 |
Camptodactyly-Ichthyosis Syndrome |
| 602612 |
Camptodactyly, Myopia, and Fibrosis of the Medial Rectus Muscle of Eye |
| 211910 |
Camptodactyly Syndrome, Guadalajara, Type I; GCS1 |
| 211920 |
Camptodactyly Syndrome, Guadalajara, Type II |
| 611929 |
Camptodactyly Syndrome, Guadalajara, Type III |
| 610474 |
Camptodactyly, Tall Stature, and Hearing Loss Syndrome |
| 211930 |
Camptodactyly with Fibrous Tissue Hyperplasia and Skeletal Dysplasia |
| 211960 |
Camptodactyly with Muscular Hypoplasia, Skeletal Dysplasia, and Abnormal Palmar Creases |
| 211990 |
Camptomelic Syndrome, Long-Limb Type |
| 607539 |
Camptosynpolydactyly, Complex |
| 131300 |
Camurati-Engelmann Disease; CAEND (1 mouse model) |
| 606631 |
Camurati-Engelmann Disease, Type 2 |
| 271900 |
Canavan Disease (3 mouse models) |
| 114450 |
Cancer, Familial, with in Vitro Radioresistance |
| 114580 |
Candidiasis, Familial, 1; CANDF1 |
| 212050 |
Candidiasis, Familial, 2; CANDF2 |
| 607644 |
Candidiasis, Familial, 3; CANDF3 |
| 613108 |
Candidiasis, Familial, 4; CANDF4 |
| 613953 |
Candidiasis, Familial, 5; CANDF5 |
| 613956 |
Candidiasis, Familial, 6; CANDF6 |
| 614162 |
Candidiasis, Familial, 7; CANDF7 |
| 114600 |
Canine Teeth, Absence of Upper Permanent |
| 239850 |
Cantu Syndrome |
| 608354 |
Capillary Malformation-Arteriovenous Malformation |
| 613089 |
Capillary Malformation of the Lower Lip, Lymphatic Malformation of Face and Neck, Asymmetry of Face and Limbs, and Partial/Generalized Overgrowth |
| 163000 |
Capillary Malformations, Congenital, 1 |
| 114700 |
Carabelli Anomaly of Maxillary Molar Teeth |
| 608307 |
Carbamoyl Phosphate Synthetase I; CPS1 |
| 237300 |
Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to (1 mouse model) |
| 212060 |
Carbimazole Sensitivity |
| 114835 |
Carboxylesterase 1; CES1 |
| 212070 |
Carboxypeptidase N Deficiency |
| 114900 |
Carcinoid Tumors, Intestinal |
| 115000 |
Cardiac Arrhythmia (1 mouse model) |
| 600919 |
Cardiac Arrhythmia, Ankyrin-B-Related |
| 115080 |
Cardiac Conduction Defect |
| 212080 |
Cardiac Lipidosis, Familial |
| 600987 |
Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies |
| 212090 |
Cardiac Septal Defects with Coarctation of the Aorta |
| 212093 |
Cardiac Valvular Defect, Developmental |
| 314400 |
Cardiac Valvular Dysplasia, X-Linked; CVD1 |
| 212100 |
Cardioauditory Syndrome of Sanchez Cascos |
| 604377 |
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1; CEMCOX1 |
| 615119 |
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2; CEMCOX2 |
| 115150 |
Cardiofaciocutaneous Syndrome (3 mouse models) |
| 212130 |
Cardiomyopathy Associated with Myopathy and Sudden Death |
| 612158 |
Cardiomyopathy, Dilated, 1aa; CMD1AA |
| 115200 |
Cardiomyopathy, Dilated, 1A; CMD1A (4 mouse models) |
| 612877 |
Cardiomyopathy, Dilated, 1bb; CMD1BB |
| 600884 |
Cardiomyopathy, Dilated, 1B; CMD1B |
| 613122 |
Cardiomyopathy, Dilated, 1cc; CMD1CC |
| 601493 |
Cardiomyopathy, Dilated, 1C; CMD1C (2 mouse models) |
| 601494 |
Cardiomyopathy, Dilated, 1D; CMD1D (3 mouse models) |
| 613172 |
Cardiomyopathy, Dilated, 1dd; CMD1DD |
| 601154 |
Cardiomyopathy, Dilated, 1E; CMD1E |
| 613252 |
Cardiomyopathy, Dilated, 1ee; CMD1EE |
| 613286 |
Cardiomyopathy, Dilated, 1ff; CMD1FF |
| 604145 |
Cardiomyopathy, Dilated, 1G; CMD1G (1 mouse model) |
| 613642 |
Cardiomyopathy, Dilated, 1gg; CMD1GG |
| 604288 |
Cardiomyopathy, Dilated, 1H; CMD1H |
| 613881 |
Cardiomyopathy, Dilated, 1hh; CMD1HH |
| 604765 |
Cardiomyopathy, Dilated, 1I; CMD1I (1 mouse model) |
| 605362 |
Cardiomyopathy, Dilated, 1J; CMD1J |
| 605582 |
Cardiomyopathy, Dilated, 1K; CMD1K |
| 606685 |
Cardiomyopathy, Dilated, 1L; CMD1L (2 mouse models) |
| 607482 |
Cardiomyopathy, Dilated, 1M; CMD1M (1 mouse model) |
| 607487 |
Cardiomyopathy, Dilated, 1N; CMD1N |
| 608569 |
Cardiomyopathy, Dilated, 1O; CMD1O |
| 609909 |
Cardiomyopathy, Dilated, 1p; CMD1P |
| 609915 |
Cardiomyopathy, Dilated, 1q; CMD1Q |
| 613424 |
Cardiomyopathy, Dilated, 1r; CMD1R (1 mouse model) |
| 613426 |
Cardiomyopathy, Dilated, 1s; CMD1S |
| 613740 |
Cardiomyopathy, Dilated, 1t; CMD1T |
| 613694 |
Cardiomyopathy, Dilated, 1u; CMD1U |
| 613697 |
Cardiomyopathy, Dilated, 1v; CMD1V |
| 611407 |
Cardiomyopathy, Dilated, 1w; CMD1W |
| 611615 |
Cardiomyopathy, Dilated, 1x; CMD1X |
| 611878 |
Cardiomyopathy, Dilated, 1y; CMD1Y |
| 611879 |
Cardiomyopathy, Dilated, 1z; CMD1Z |
| 611880 |
Cardiomyopathy, Dilated, 2A; CMD2A |
| 614672 |
Cardiomyopathy, Dilated, 2B; CMD2B |
| 302045 |
Cardiomyopathy, Dilated, 3b; CMD3B (2 mouse models) |
| 212112 |
Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism |
| 605676 |
Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma |
| 608758 |
Cardiomyopathy, Familial Hypertrophic, 10; CMH10 (1 mouse model) |
| 612098 |
Cardiomyopathy, Familial Hypertrophic, 11; CMH11 |
| 612124 |
Cardiomyopathy, Familial Hypertrophic, 12; CMH12 (1 mouse model) |
| 613243 |
Cardiomyopathy, Familial Hypertrophic, 13; CMH13 |
| 613251 |
Cardiomyopathy, Familial Hypertrophic, 14; CMH14 (6 mouse models) |
| 613255 |
Cardiomyopathy, Familial Hypertrophic, 15; CMH15 |
| 613838 |
Cardiomyopathy, Familial Hypertrophic, 16; CMH16 |
| 613873 |
Cardiomyopathy, Familial Hypertrophic, 17; CMH17 |
| 613874 |
Cardiomyopathy, Familial Hypertrophic, 18; CMH18 |
| 613875 |
Cardiomyopathy, Familial Hypertrophic, 19; CMH19 |
| 192600 |
Cardiomyopathy, Familial Hypertrophic, 1; CMH1 (1 mouse model) |
| 613876 |
Cardiomyopathy, Familial Hypertrophic, 20; CMH20 |
| 614676 |
Cardiomyopathy, Familial Hypertrophic, 21; CMH21 |
| 115195 |
Cardiomyopathy, Familial Hypertrophic, 2; CMH2 (5 mouse models) |
| 115196 |
Cardiomyopathy, Familial Hypertrophic, 3; CMH3 (1 mouse model) |
| 115197 |
Cardiomyopathy, Familial Hypertrophic, 4; CMH4 (4 mouse models) |
| 600858 |
Cardiomyopathy, Familial Hypertrophic, 6; CMH6 (1 mouse model) |
| 613690 |
Cardiomyopathy, Familial Hypertrophic, 7; CMH7 |
| 608751 |
Cardiomyopathy, Familial Hypertrophic, 8; CMH8 (1 mouse model) |
| 613765 |
Cardiomyopathy, Familial Hypertrophic, 9; CMH9 |
| 115210 |
Cardiomyopathy, Familial Restrictive, 1; RCM1 |
| 609578 |
Cardiomyopathy, Familial Restrictive, 2; RCM2 |
| 612422 |
Cardiomyopathy, Familial Restrictive, 3; RCM3 |
| 300829 |
Cardiomyopathy, Fatal Fetal, Due to Myocardial Calcification |
| 500000 |
Cardiomyopathy, Infantile Histiocytoid |
| 606842 |
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods |
| 212135 |
Cardioskeletal Syndrome, Kuwaiti Type |
| 114650 |
Car Factor Deficiency |
| 160980 |
Carney Complex, Type 1; CNC1 (4 mouse models) |
| 605244 |
Carney Complex, Type 2; CNC2 |
| 608837 |
Carney Complex Variant |
| 604287 |
Carney Triad |
| 606175 |
Carnitine Acetyltransferase Deficiency |
| 212138 |
Carnitine-Acylcarnitine Translocase Deficiency |
| 212160 |
Carnitine Deficiency, Myopathic |
| 212140 |
Carnitine Deficiency, Systemic Primary; CDSP (1 mouse model) |
| 255120 |
Carnitine Palmitoyltransferase I Deficiency (1 mouse model) |
| 600649 |
Carnitine Palmitoyltransferase II Deficiency, Infantile |
| 255110 |
Carnitine Palmitoyltransferase II Deficiency, Late-Onset |
| 608836 |
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal |
| 212200 |
Carnosinemia |
| 600643 |
Caroli Disease, Isolated |
| 604172 |
Caronte |
| 609338 |
Carotid Intimal Medial Thickness 1 |
| 608447 |
Carotid Intimal Medial Thickness 2 |
| 115400 |
Carpal Displacement |
| 115430 |
Carpal Tunnel Syndrome; CTS1 |
| 201000 |
Carpenter Syndrome 1; CRPT1 |
| 614976 |
Carpenter Syndrome 2; CRPT2 (1 mouse model) |
| 250250 |
Cartilage-Hair Hypoplasia; CHH |
| 607271 |
CASPase 8 Deficiency (1 mouse model) |
| 115645 |
Cataract, Aberrant Oral Frenula, and Growth Retardation |
| 609026 |
Cataract, Age-Related Cortical, 1; ARCC1 |
| 613020 |
Cataract, Age-Related Cortical, 2; ARCC2 (1 mouse model) |
| 601371 |
Cataract, Age-Related Nuclear |
| 212400 |
Cataract and Congenital Ichthyosis |
| 115650 |
Cataract, Anterior Polar, 1; CTAA1 (5 mouse models) |
| 601202 |
Cataract, Anterior Polar, 2; CTAA2 |
| 212710 |
Cataract-Ataxia-Deafness-Retardation Syndrome |
| 300619 |
Cataract, Ataxia, Short Stature, and Mental Retardation |
| 604219 |
Cataract, Autosomal Dominant (42 mouse models) |
| 611597 |
Cataract, Autosomal Dominant, Multiple Types 1 |
| 610019 |
Cataract, Autosomal Recessive Congenital 2; CATC2 |
| 612968 |
Cataract, Autosomal Recessive Congenital 3; CATC3 |
| 613887 |
Cataract, Autosomal Recessive Congenital 4; CATC4 |
| 614691 |
Cataract, Autosomal Recessive Congenital 5; CATC5 |
| 605749 |
Cataract, Autosomal Recessive, Early-Onset, Pulverulent (2 mouse models) |
| 605728 |
Cataract, Central Saccular, with Sutural Opacities |
| 115660 |
Cataract, Congenital, Cerulean Type, 1; CCA1 |
| 601547 |
Cataract, Congenital, Cerulean Type, 2; CCA2 (3 mouse models) |
| 608983 |
Cataract, Congenital, Cerulean Type, 3; CCA3 |
| 614422 |
Cataract, Congenital, Cerulean Type, 5; CCA5 |
| 609376 |
Cataract, Congenital Nuclear, Autosomal Recessive 1; CATCN1 |
| 609741 |
Cataract, Congenital Nuclear, Autosomal Recessive 2; CATCN2 |
| 611544 |
Cataract, Congenital Nuclear, Autosomal Recessive 3; CATCN3 |
| 212500 |
Cataract, Congenital or Juvenile |
| 115665 |
Cataract, Congenital, Volkmann Type; CCV |
| 607674 |
Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy |
| 302200 |
Cataract, Congenital, X-Linked; CXN |
| 600881 |
Cataract, Congenital Zonular, with Sutural Opacities; CCZS (2 mouse models) |
| 604307 |
Cataract, Coppock-Like; CCL (3 mouse models) |
| 611391 |
Cataract, Cortical, Juvenile-Onset |
| 115700 |
Cataract, Crystalline Aculeiform (2 mouse models) |
| 115800 |
Cataract, Crystalline Coralliform |
| 115900 |
Cataract, Floriform |
| 612018 |
Cataract, Juvenile, with Microcornea and Glucosuria |
| 116800 |
Cataract, Lamellar (3 mouse models) |
| 610425 |
Cataract, Lamellar 2 |
| 116100 |
Cataract, Membranous |
| 212540 |
Cataract, Microcephaly, Failure to Thrive, Kyphoscoliosis Syndrome |
| 116150 |
Cataract-Microcornea Syndrome |
| 601286 |
Cataract, Nonnuclear Polymorphic Congenital, Autosomal Dominant |
| 116300 |
Cataract, Nuclear Diffuse Nonprogressive (1 mouse model) |
| 607304 |
Cataract, Nuclear Progressive |
| 116400 |
Cataract, Nuclear Total |
| 116600 |
Cataract, Posterior Polar, 1; CTPP1 |
| 613763 |
Cataract, Posterior Polar, 2; CTPP2 |
| 605387 |
Cataract, Posterior Polar, 3; CTPP3 |
| 610623 |
Cataract, Posterior Polar, 4; CTPP4 |
| 610634 |
Cataract, Posterior Polar, 5; CTPP5 |
| 610202 |
Cataract, Pulverulent, Juvenile-Onset (1 mouse model) |
| 601088 |
Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation |
| 607133 |
Cataract, Sutural, with Punctate and Cerulean Opacities |
| 116700 |
Cataract, Total Congenital; CC |
| 116200 |
Cataract, Zonular Pulverulent 1; CZP1 (3 mouse models) |
| 601885 |
Cataract, Zonular Pulverulent 3; CZP3 |
| 116850 |
Catatrichy |
| 116790 |
Catechol-O-Methyltransferase; COMT |
| 302380 |
Catel-Manzke Syndrome |
| 115470 |
Cat Eye Syndrome; CES |
| 607864 |
Caudal Duplication Anomaly |
| 611543 |
Cavitary Optic Disc Anomalies |
| 125520 |
Cayler Cardiofacial Syndrome |
| 186830 |
CD3 Antigen, Epsilon Subunit; CD3E |
| 186740 |
CD3 Antigen, Gamma Subunit; CD3G |
| 601083 |
CD4/CD8 T-Cell Ratio |
| 612300 |
Cd59 Deficiency |
| 608957 |
CD8 Deficiency, Familial |
| 603116 |
Cdags Syndrome |
| 116870 |
Celiac Artery Stenosis From Compression By Median Arcuate Ligament of Diaphragm |
| 212750 |
Celiac Disease; CD |
| 612008 |
Celiac Disease, Susceptibility to, 10; CELIAC10 |
| 612009 |
Celiac Disease, Susceptibility to, 11; CELIAC11 |
| 612010 |
Celiac Disease, Susceptibility to, 12; CELIAC12 |
| 612011 |
Celiac Disease, Susceptibility to, 13; CELIAC13 |
| 609754 |
Celiac Disease, Susceptibility to, 2; CELIAC2 |
| 609755 |
Celiac Disease, Susceptibility to, 3; CELIAC3 |
| 609753 |
Celiac Disease, Susceptibility to, 4; CELIAC4 |
| 607202 |
Celiac Disease, Susceptibility to, 5; CELIAC5 |
| 611598 |
Celiac Disease, Susceptibility to, 6; CELIAC6 |
| 612005 |
Celiac Disease, Susceptibility to, 7; CELIAC7 |
| 612006 |
Celiac Disease, Susceptibility to, 8; CELIAC8 |
| 612007 |
Celiac Disease, Susceptibility to, 9; CELIAC9 |
| 212780 |
Cenani-Lenz Syndactyly Syndrome; CLSS (1 mouse model) |
| 217600 |
Central Cloudy Dystrophy of Francois; CCDF |
| 117000 |
Central Core Disease of Muscle (2 mouse models) |
| 209880 |
Central Hypoventilation Syndrome, Congenital; CCHS (2 mouse models) |
| 302400 |
Central Incisors, Absence of |
| 117100 |
Centralopathic Epilepsy |
| 212800 |
Cephalin Lipidosis |
| 212835 |
Cerebellar Ataxia and Ectodermal Dysplasia |
| 605672 |
Cerebellar Ataxia and Hypergonadotropic Hypogonadism |
| 212840 |
Cerebellar Ataxia and Hypogonadotropic Hypogonadism |
| 212850 |
Cerebellar Ataxia and Neurosensory Deafness |
| 601338 |
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, and Sensorineural Hearing Loss |
| 212890 |
Cerebellar Ataxia, Benign, with Thermoanalgesia |
| 601238 |
Cerebellar Ataxia, Cayman Type; ATCAY |
| 604121 |
Cerebellar Ataxia, Deafness, and Narcolepsy |
| 212895 |
Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes; EOCA |
| 224050 |
Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1; CAMRQ1 |
| 610185 |
Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 2; CAMRQ2 |
| 613227 |
Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 3; CAMRQ3 |
| 614575 |
Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome; |
| 614756 |
Cerebellar Ataxia, Nonprogressive, with Mental Retardation; CANPMR |
| 602197 |
Cerebellar Degeneration-Related Autoantigen 3 |
| 213000 |
Cerebellar Hypoplasia |
| 213002 |
Cerebellar Hypoplasia with Endosteal Sclerosis |
| 213010 |
Cerebellar Vermis Aplasia with Associated Features Suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome |
| 213100 |
Cerebelloparenchymal Disorder II; CPD2 |
| 213400 |
Cerebelloparenchymal Disorder V; CPD5 |
| 601853 |
Cerebellotrigeminal Dermal Dysplasia (1 mouse model) |
| 605714 |
Cerebral Amyloid Angiopathy, App-Related (7 mouse models) |
| 105150 |
Cerebral Amyloid Angiopathy, Cst3-Related |
| 176500 |
Cerebral Amyloid Angiopathy, Itm2b-Related, 1 (2 mouse models) |
| 117300 |
Cerebral Amyloid Angiopathy, Itm2b-Related, 2 (4 mouse models) |
| 213500 |
Cerebral Angiopathy, Dysphoric |
| 125310 |
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy; CADASIL (5 mouse models) |
| 600142 |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy; CARASIL |
| 603284 |
Cerebral Cavernous Malformations 2; CCM2 (2 mouse models) |
| 603285 |
Cerebral Cavernous Malformations 3; CCM3 (3 mouse models) |
| 116860 |
Cerebral Cavernous Malformations; CCM (3 mouse models) |
| 300864 |
Cerebral-Cerebellar-Coloboma Syndrome, X-Linked |
| 609528 |
Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome |
| 213820 |
Cerebral Malformation, Seizures, Hypertrichosis, and Overlapping Fingers |
| 605388 |
Cerebral Palsy, Ataxic, Autosomal Recessive |
| 603513 |
Cerebral Palsy, Spastic Quadriplegic, 1; CPSQ1 |
| 612900 |
Cerebral Palsy, Spastic Quadriplegic, 2; CPSQ2 |
| 117600 |
Cerebral Sarcoma |
| 302700 |
Cerebral Sclerosis, Diffuse, Scholz Type |
| 213900 |
Cerebral Sclerosis Similar to Pelizaeus-Merzbacher Disease |
| 213950 |
Cerebrocortical Degeneration of Infancy |
| 117650 |
Cerebrocostomandibular Syndrome |
| 601390 |
Cerebrofacioarticular Syndrome |
| 213980 |
Cerebrofaciothoracic Dysplasia |
| 608578 |
Cerebrofrontofacial Syndrome |
| 214150 |
Cerebrooculofacioskeletal Syndrome 1; COFS1 (1 mouse model) |
| 610756 |
Cerebrooculofacioskeletal Syndrome 2; COFS2 |
| 610758 |
Cerebrooculofacioskeletal Syndrome 4; COFS4 |
| 605627 |
Cerebrooculonasal Syndrome |
| 609345 |
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula |
| 612199 |
Cerebroretinal Microangiopathy with Calcifications and Cysts; CRMCC |
| 213700 |
Cerebrotendinous Xanthomatosis; CTX |
| 610127 |
Ceroid Lipofuscinosis, Neuronal, 10; CLN10 (1 mouse model) |
| 614706 |
Ceroid Lipofuscinosis, Neuronal, 11; CLN11 |
| 256730 |
Ceroid Lipofuscinosis, Neuronal, 1; CLN1 (1 mouse model) |
| 204500 |
Ceroid Lipofuscinosis, Neuronal, 2; CLN2 (3 mouse models) |
| 204200 |
Ceroid Lipofuscinosis, Neuronal, 3; CLN3 (10 mouse models) |
| 204300 |
Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive; CLN4A |
| 162350 |
Ceroid Lipofuscinosis, Neuronal, 4b, Autosomal Dominant; CLN4B |
| 256731 |
Ceroid Lipofuscinosis, Neuronal, 5; CLN5 (1 mouse model) |
| 601780 |
Ceroid Lipofuscinosis, Neuronal, 6; CLN6 (1 mouse model) |
| 610951 |
Ceroid Lipofuscinosis, Neuronal, 7; CLN7 |
| 600143 |
Ceroid Lipofuscinosis, Neuronal, 8; CLN8 (4 mouse models) |
| 610003 |
Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant |
| 609055 |
Ceroid Lipofuscinosis, Neuronal, 9; CLN9 |
| 214200 |
Ceroid Storage Disease |
| 603956 |
Cervical Cancer |
| 117850 |
Cervical Hypertrichosis with Underlying Kyphoscoliosis |
| 117900 |
Cervical Rib |
| 601389 |
Cervical Ribs, Sprengel Anomaly, Anal Atresia, and Urethral Obstruction |
| 214290 |
Cervical Vertebrae, Agenesis of |
| 118000 |
Cervical Vertebral Bridge |
| 118005 |
Cervical Vertebral Dysplasia |
| 614809 |
Cfhr5 Deficiency |
| 275630 |
Chanarin-Dorfman Syndrome; CDS (1 mouse model) |
| 214350 |
CHANDS |
| 118300 |
Charcot-Marie-Tooth Disease and Deafness |
| 118210 |
Charcot-Marie-Tooth Disease, Axonal, Type 2a1; CMT2A1 (1 mouse model) |
| 609260 |
Charcot-Marie-Tooth Disease, Axonal, Type 2A2; CMT2A2 (1 mouse model) |
| 605588 |
Charcot-Marie-Tooth Disease, Axonal, Type 2B1; CMT2B1 (1 mouse model) |
| 605589 |
Charcot-Marie-Tooth Disease, Axonal, Type 2B2; CMT2B2 |
| 600882 |
Charcot-Marie-Tooth Disease, Axonal, Type 2B; CMT2B |
| 601472 |
Charcot-Marie-Tooth Disease, Axonal, Type 2D; CMT2D (3 mouse models) |
| 607684 |
Charcot-Marie-Tooth Disease, Axonal, Type 2E; CMT2E (2 mouse models) |
| 606595 |
Charcot-Marie-Tooth Disease, Axonal, Type 2F; CMT2F (1 mouse model) |
| 608591 |
Charcot-Marie-Tooth Disease, Axonal, Type 2G; CMT2G |
| 607731 |
Charcot-Marie-Tooth Disease, Axonal, Type 2H; CMT2H |
| 607677 |
Charcot-Marie-Tooth Disease, Axonal, Type 2I; CMT2I |
| 607736 |
Charcot-Marie-Tooth Disease, Axonal, Type 2J; CMT2J |
| 607831 |
Charcot-Marie-Tooth Disease, Axonal, Type 2K; CMT2K |
| 608673 |
Charcot-Marie-Tooth Disease, Axonal, Type 2L; CMT2L |
| 613287 |
Charcot-Marie-Tooth Disease, Axonal, Type 2n; CMT2N |
| 614228 |
Charcot-Marie-Tooth Disease, Axonal, Type 2o; CMT2O |
| 614436 |
Charcot-Marie-Tooth Disease, Axonal, Type 2p; CMT2P |
| 615025 |
Charcot-Marie-Tooth Disease, Axonal, Type 2q; CMT2Q |
| 607706 |
Charcot-Marie-Tooth Disease, Axonal, with Vocal Cord Paresis, Autosomal Recessive |
| 118220 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1A; CMT1A (5 mouse models) |
| 118200 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1B; CMT1B (2 mouse models) |
| 601098 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1C; CMT1C |
| 607678 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1D; CMT1D |
| 607734 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1F; CMT1F |
| 614895 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f; CMT4F |
| 606483 |
Charcot-Marie-Tooth Disease, Dominant Intermediate A; CMTDIA |
| 606482 |
Charcot-Marie-Tooth Disease, Dominant Intermediate B; CMTDIB |
| 608323 |
Charcot-Marie-Tooth Disease, Dominant Intermediate C; CMTDIC |
| 607791 |
Charcot-Marie-Tooth Disease, Dominant Intermediate D; CMTDID |
| 614455 |
Charcot-Marie-Tooth Disease, Dominant Intermediate E; CMTDIE |
| 118230 |
Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type |
| 608340 |
Charcot-Marie-Tooth Disease, Recessive Intermediate A; CMTRIA |
| 613641 |
Charcot-Marie-Tooth Disease, Recessive Intermediate B; CMTRIB |
| 214400 |
Charcot-Marie-Tooth Disease, Type 4A; CMT4A |
| 601382 |
Charcot-Marie-Tooth Disease, Type 4b1; CMT4B1 (2 mouse models) |
| 604563 |
Charcot-Marie-Tooth Disease, Type 4b2; CMT4B2 (2 mouse models) |
| 601596 |
Charcot-Marie-Tooth Disease, Type 4c; CMT4C (1 mouse model) |
| 601455 |
Charcot-Marie-Tooth Disease, Type 4D; CMT4D (1 mouse model) |
| 609311 |
Charcot-Marie-Tooth Disease, Type 4h; CMT4H (1 mouse model) |
| 611228 |
Charcot-Marie-Tooth Disease, Type 4j; CMT4J (2 mouse models) |
| 118301 |
Charcot-Marie-Tooth Disease with Ptosis and Parkinsonism |
| 302800 |
Charcot-Marie-Tooth Disease, X-Linked Dominant, 1; CMTX1 (4 mouse models) |
| 302801 |
Charcot-Marie-Tooth Disease, X-Linked Recessive, 2; CMTX2 |
| 302802 |
Charcot-Marie-Tooth Disease, X-Linked Recessive, 3; CMTX3 |
| 311070 |
Charcot-Marie-Tooth Disease, X-Linked Recessive, 5; CMTX5 |
| 302900 |
Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined |
| 302803 |
Charcot-Marie-Tooth Peroneal Muscular Atrophy, X-Linked, with Aplasia Cutis Congenita |
| 302905 |
CHARGE-Like Syndrome, X-Linked |
| 214800 |
CHARGE Syndrome (5 mouse models) |
| 169100 |
Char Syndrome (1 mouse model) |
| 604373 |
Checkpoint Kinase 2, S. Pombe, Homolog Of; CHEK2 |
| 214500 |
Chediak-Higashi Syndrome; CHS (8 mouse models) |
| 118330 |
Cheilitis Glandularis |
| 118350 |
Chemodectoma, Intraabdominal, with Cutaneous Angiolipomas |
| 158105 |
Chemokine, Cc Motif, Ligand 2; CCL2 |
| 118400 |
Cherubism (1 mouse model) |
| 118420 |
Chiari Malformation Type I |
| 207950 |
Chiari Malformation Type II |
| 610448 |
Chilblain Lupus 1; CHBL1 |
| 614415 |
Chilblain Lupus 2; CHBL2 |
| 614122 |
Chitotriosidase Deficiency; CHITD |
| 515000 |
Chloramphenicol Toxicity |
| 118430 |
Chlorpropamide-Alcohol Flushing; CPAF |
| 613611 |
Choanal Atresia and Lymphedema |
| 608911 |
Choanal Atresia, Posterior; PCA |
| 613806 |
Cholangitis, Primary Sclerosing; PSC |
| 243300 |
Cholestasis, Benign Recurrent Intrahepatic, 1; BRIC1 |
| 605479 |
Cholestasis, Benign Recurrent Intrahepatic, 2; BRIC2 |
| 147480 |
Cholestasis, Intrahepatic, of Pregnancy, 1; ICP1 |
| 614972 |
Cholestasis, Intrahepatic, of Pregnancy 3; ICP3 |
| 214900 |
Cholestasis-Lymphedema Syndrome |
| 211600 |
Cholestasis, Progressive Familial Intrahepatic, 1; PFIC1 |
| 601847 |
Cholestasis, Progressive Familial Intrahepatic, 2; PFIC2 |
| 602347 |
Cholestasis, Progressive Familial Intrahepatic, 3; PFIC3 |
| 214980 |
Cholestasis with Gallstone, Ataxia, and Visual Disturbance |
| 604183 |
Cholesteatoma, Congenital |
| 604595 |
Cholesterol Level Quantitative Trait Locus 1 |
| 215030 |
Cholesterol Pneumonia |
| 600668 |
Chondrocalcinosis 1; CCAL1 |
| 118600 |
Chondrocalcinosis 2; CCAL2 |
| 118610 |
Chondrocalcinosis Due to Apatite Crystal Deposition |
| 609441 |
Chondrodysplasia, Acromesomelic, with Genital Anomalies |
| 215045 |
Chondrodysplasia, Blomstrand Type; BOCD |
| 215050 |
Chondrodysplasia Calcificans Metaphysealis |
| 200700 |
Chondrodysplasia, Grebe Type |
| 601376 |
Chondrodysplasia, Lethal, with Long Bone Angulation and Mixed Bone Density |
| 613320 |
Chondrodysplasia, Megarbane-Dagher-Melki Type |
| 600092 |
Chondrodysplasia-Pseudohermaphroditism Syndrome |
| 302950 |
Chondrodysplasia Punctata 1, X-Linked Recessive; CDPX1 |
| 302960 |
Chondrodysplasia Punctata 2, X-Linked Dominant; CDPX2 (2 mouse models) |
| 118650 |
Chondrodysplasia Punctata, Autosomal Dominant |
| 602497 |
Chondrodysplasia Punctata, Brachytelephalangic, Autosomal |
| 215105 |
Chondrodysplasia Punctata Syndrome |
| 118651 |
Chondrodysplasia Punctata, Tibia-Metacarpal Type |
| 614078 |
Chondrodysplasia with Joint Dislocations, Gpapp Type |
| 300863 |
Chondrodysplasia with Platyspondyly, Distinctive Brachydactyly, Hydrocephaly, and Microphthalmia |
| 215250 |
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome |
| 118670 |
Chondronectin |
| 215300 |
Chondrosarcoma |
| 612237 |
Chondrosarcoma, Extraskeletal Myxoid |
| 215400 |
Chordoma, Susceptibility To; CHDM |
| 215450 |
Chorea, Benign Familial |
| 118700 |
Chorea, Benign Hereditary; BHC |
| 601372 |
Chorea, Remitting, with Nystagmus and Cataract |
| 200150 |
Choreoacanthocytosis; CHAC (1 mouse model) |
| 118750 |
Choreoathetosis, Familial Inverted |
| 610978 |
Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress |
| 600790 |
Chorioretinal Atrophy, Progressive Bifocal |
| 215470 |
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism |
| 215500 |
Choroidal Dystrophy, Central Areolar 1; CACD1 |
| 613105 |
Choroidal Dystrophy, Central Areolar 2; CACD2 |
| 613144 |
Choroidal Dystrophy, Central Areolar 3; CACD3 |
| 118865 |
Choroidal Osteoma, Bilateral |
| 303100 |
Choroideremia; CHM (4 mouse models) |
| 303110 |
Choroideremia, Deafness, and Mental Retardation |
| 215480 |
Choroid Plexus Calcification and Mental Retardation |
| 215510 |
Chromosomal Instability with Tissue-Specific Radiosensitivity |
| 612242 |
Chromosome 10q23 Deletion Syndrome |
| 609625 |
Chromosome 10q26 Deletion Syndrome |
| 613884 |
Chromosome 13q14 Deletion Syndrome |
| 613457 |
Chromosome 14q11-Q22 Deletion Syndrome |
| 608636 |
Chromosome 15q11-Q13 Duplication Syndrome (2 mouse models) |
| 612001 |
Chromosome 15q13.3 Deletion Syndrome |
| 613406 |
Chromosome 15q24 Deletion Syndrome |
| 614294 |
Chromosome 15q25 Deletion Syndrome |
| 612626 |
Chromosome 15q26-Qter Deletion Syndrome |
| 613444 |
Chromosome 16p11.2 Deletion Syndrome, 220-Kb |
| 611913 |
Chromosome 16p11.2 Deletion Syndrome, 593-Kb |
| 614671 |
Chromosome 16p11.2 Duplication Syndrome |
| 136570 |
Chromosome 16p12.1 Deletion Syndrome, 520-Kb |
| 613604 |
Chromosome 16p12.2-P11.2 Deletion Syndrome, 7.1- to 8.7-Mb |
| 610543 |
Chromosome 16p13.3 Deletion Syndrome, Proximal |
| 613458 |
Chromosome 16p13.3 Duplication Syndrome |
| 614541 |
Chromosome 16q22 Deletion Syndrome |
| 613776 |
Chromosome 17p13.1 Deletion Syndrome |
| 613215 |
Chromosome 17p13.3 Duplication Syndrome |
| 613675 |
Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb |
| 614527 |
Chromosome 17q12 Deletion Syndrome |
| 614526 |
Chromosome 17q12 Duplication Syndrome |
| 613533 |
Chromosome 17q21.31 Duplication Syndrome |
| 613355 |
Chromosome 17q23.1-Q23.2 Deletion Syndrome |
| 613618 |
Chromosome 17q23.1-Q23.2 Duplication Syndrome |
| 146390 |
Chromosome 18p Deletion Syndrome |
| 609334 |
Chromosome 18 Pericentric Inversion |
| 601808 |
Chromosome 18q Deletion Syndrome |
| 613638 |
Chromosome 19p13.13 Deletion Syndrome |
| 613026 |
Chromosome 19q13.11 Deletion Syndrome |
| 613735 |
Chromosome 1p32-P31 Deletion Syndrome |
| 607872 |
Chromosome 1p36 Deletion Syndrome (1 mouse model) |
| 612474 |
Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb |
| 612475 |
Chromosome 1q21.1 Duplication Syndrome |
| 612530 |
Chromosome 1q41-Q42 Deletion Syndrome |
| 612337 |
Chromosome 1q43-Q44 Deletion Syndrome (1 mouse model) |
| 611867 |
Chromosome 22q11.2 Deletion Syndrome, Distal (2 mouse models) |
| 608363 |
Chromosome 22q11.2 Duplication Syndrome |
| 606232 |
Chromosome 22q13.3 Deletion Syndrome |
| 613564 |
Chromosome 2p12-P11.2 Deletion Syndrome |
| 612513 |
Chromosome 2p16.1-P15 Deletion Syndrome |
| 613681 |
Chromosome 2q31.1 Duplication Syndrome |
| 612345 |
Chromosome 2q31.2 Deletion Syndrome |
| 612313 |
Chromosome 2q32-Q33 Deletion Syndrome |
| 613792 |
Chromosome 3pter-P25 Deletion Syndrome |
| 609425 |
Chromosome 3q29 Deletion Syndrome |
| 611936 |
Chromosome 3q29 Duplication Syndrome |
| 613509 |
Chromosome 4q21 Deletion Syndrome |
| 613603 |
Chromosome 4q32.1-Q32.2 Triplication Syndrome |
| 613174 |
Chromosome 5p13 Duplication Syndrome |
| 153550 |
Chromosome 5q Deletion Syndrome (2 mouse models) |
| 612582 |
Chromosome 6pter-P24 Deletion Syndrome |
| 613544 |
Chromosome 6q11-Q14 Deletion Syndrome |
| 612863 |
Chromosome 6q24-Q25 Deletion Syndrome |
| 613729 |
Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-Mb |
| 613523 |
Chromosome 8p11 Myeloproliferative Syndrome |
| 600257 |
Chromosome 8q12.1-Q21.2 Deletion Syndrome |
| 614230 |
Chromosome 8q21.11 Deletion Syndrome |
| 158170 |
Chromosome 9p Deletion Syndrome (2 mouse models) |
| 300801 |
Chromosome Xp11.23-P11.22 Duplication Syndrome |
| 300578 |
Chromosome Xp11.3 Deletion Syndrome |
| 300679 |
Chromosome Xp21 Deletion Syndrome |
| 300830 |
Chromosome Xp22 Deletion Syndrome |
| 300869 |
Chromosome Xq27.3-Q28 Duplication Syndrome |
| 300475 |
Chromosome Xq28 Deletion Syndrome |
| 300815 |
Chromosome Xq28 Duplication Syndrome |
| 259680 |
Chronic Recurrent Multifocal Osteomyelitis; CRMO (1 mouse model) |
| 604213 |
Chudley-Mccullough Syndrome; CMCS |
| 118830 |
Chylomicronemia, Familial, Due to Circulating Inhibitor of Lipoprotein Lipase |
| 246700 |
Chylomicron Retention Disease; CMRD (2 mouse models) |
| 603523 |
Chylothorax, Congenital (2 mouse models) |
| 215518 |
Ciliary Discoordination Due to Random Ciliary Orientation |
| 612518 |
Ciliary Dyskinesia, Primary, 10; CILD10 |
| 612649 |
Ciliary Dyskinesia, Primary, 11; CILD11 |
| 612650 |
Ciliary Dyskinesia, Primary, 12; CILD12 |
| 613193 |
Ciliary Dyskinesia, Primary, 13; CILD13 |
| 613807 |
Ciliary Dyskinesia, Primary, 14; CILD14 |
| 613808 |
Ciliary Dyskinesia, Primary, 15; CILD15 |
| 614017 |
Ciliary Dyskinesia, Primary, 16; CILD16 |
| 614679 |
Ciliary Dyskinesia, Primary, 17; CILD17 |
| 614874 |
Ciliary Dyskinesia, Primary, 18; CILD18 |
| 614935 |
Ciliary Dyskinesia, Primary, 19; CILD19 |
| 244400 |
Ciliary Dyskinesia, Primary, 1; CILD1 (32 mouse models) |
| 615067 |
Ciliary Dyskinesia, Primary, 20; CILD20 |
| 606763 |
Ciliary Dyskinesia, Primary, 2; CILD2 |
| 608644 |
Ciliary Dyskinesia, Primary, 3; CILD3 (2 mouse models) |
| 608646 |
Ciliary Dyskinesia, Primary, 4; CILD4 |
| 608647 |
Ciliary Dyskinesia, Primary, 5; CILD5 |
| 610852 |
Ciliary Dyskinesia, Primary, 6; CILD6 |
| 611884 |
Ciliary Dyskinesia, Primary, 7; CILD7 |
| 612274 |
Ciliary Dyskinesia, Primary, 8; CILD8 |
| 612444 |
Ciliary Dyskinesia, Primary, 9; CILD9 |
| 242670 |
Ciliary Dyskinesia with Defective Radial Spokes |
| 242680 |
Ciliary Dyskinesia with Excessively Long Cilia |
| 215520 |
Ciliary Dyskinesia with Transposition of Ciliary Microtubules |
| 607115 |
CINCA Syndrome; CINCA (1 mouse model) |
| 215550 |
Circumvallate Placenta Syndrome |
| 215600 |
Cirrhosis, Familial |
| 118900 |
Cirrhosis, Familial |
| 215700 |
Citrullinemia, Classic (6 mouse models) |
| 603471 |
Citrullinemia, Type II, Adult-Onset; CTLN2 |
| 605814 |
Citrullinemia, Type II, Neonatal-Onset (1 mouse model) |
| 215720 |
Citrulline Transport Defect |
| 300831 |
Ck Syndrome |
| 300602 |
Clark-Baraitser Syndrome |
| 118980 |
Clavicle, Pseudarthrosis of, Congenital |
| 605040 |
Clavicular Hypoplasia, Zygomatic Arch Hypoplasia, and Micrognathia |
| 119000 |
Cleft Chin |
| 215800 |
Cleft Larynx, Posterior |
| 215850 |
Cleft-Limb-Heart Malformation Syndrome |
| 225060 |
Cleft Lip/Palate-Ectodermal Dysplasia Syndrome; CLPED1 |
| 216100 |
Cleft Lip/Palate with Abnormal Thumbs and Microcephaly |
| 601165 |
Cleft Lip/Palate with Characteristic Facies, Intestinal Malrotation, and Lethal Congenital Heart Disease |
| 155145 |
Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa |
| 600460 |
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly |
| 216300 |
Cleft Palate, Deafness, and Oligodontia |
| 119540 |
Cleft Palate, Isolated; CPI (1 mouse model) |
| 609466 |
Cleft Palate, Midfacial Hypoplasia, Triangular Facies, and Sensorineural Hearing Loss |
| 303400 |
Cleft Palate, X-Linked; CPX (2 mouse models) |
| 119570 |
Cleft Soft Palate |
| 119600 |
Cleidocranial Dysplasia; CCD (6 mouse models) |
| 216330 |
Cleidocranial Dysplasia, Recessive Form |
| 216340 |
Cleidocranial Dysplasia with Micrognathia, Absent Thumbs, and Distal Aphalangia |
| 119650 |
Cleidorhizomelic Syndrome |
| 129500 |
Clouston Syndrome |
| 119800 |
Clubfoot, Congenital, with or without Deficiency of Long Bones and/or Mirror-Image Polydactyly; CCF (11 mouse models) |
| 119915 |
Cluster Headache, Familial |
| 216360 |
COACH Syndrome |
| 120000 |
Coarctation of Aorta |
| 300216 |
Coats Disease |
| 120040 |
Cochleosaccular Degeneration with Progressive Cataracts |
| 216400 |
Cockayne Syndrome, Type A; CSA |
| 133540 |
Cockayne Syndrome, Type B; CSB (3 mouse models) |
| 216411 |
Cockayne Syndrome, Type III |
| 613630 |
Cocoon Syndrome |
| 600373 |
CODAS Syndrome |
| 607426 |
Coenzyme Q10 Deficiency, Primary, 1; COQ10D1 |
| 614651 |
Coenzyme Q10 Deficiency, Primary, 2; COQ10D2 |
| 614652 |
Coenzyme Q10 Deficiency, Primary, 3; COQ10D3 |
| 612016 |
Coenzyme Q10 Deficiency, Primary, 4; COQ10D4 |
| 614654 |
Coenzyme Q10 Deficiency, Primary, 5; COQ10D5 |
| 614650 |
Coenzyme Q10 Deficiency, Primary, 6; COQ10D6 |
| 303600 |
Coffin-Lowry Syndrome; CLS (3 mouse models) |
| 135900 |
Coffin-Siris Syndrome; CSS |
| 300082 |
Cognitive Function 1, Social; CGF1 |
| 614306 |
Cognitive Impairment with or without Cerebellar Ataxia; CIAT |
| 216550 |
Cohen Syndrome; COH1 |
| 120080 |
Colchicine Resistance |
| 272430 |
Cold-Induced Sweating Syndrome 1; CISS1 |
| 610313 |
Cold-Induced Sweating Syndrome 2; CISS2 |
| 115250 |
Collagenoma, Familial Cutaneous |
| 216700 |
Collagenosis, Familial Reactive Perforating; RPC |
| 120150 |
Collagen, Type I, Alpha-1; COL1A1 |
| 120140 |
Collagen, Type II, Alpha-1; COL2A1 |
| 609363 |
Colloid Cysts of Third Ventricle |
| 280000 |
Coloboma, Congenital Heart Disease, Ichthyosiform Dermatosis, Mental Retardation, and Ear Anomalies Syndrome; CHIME |
| 601794 |
Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome |
| 120200 |
Coloboma, Ocular |
| 216820 |
Coloboma, Ocular |
| 120300 |
Coloboma of Macula |
| 216800 |
Coloboma of Macula and Skeletal Anomalies |
| 120400 |
Coloboma of Macula with Type B Brachydactyly |
| 120430 |
Coloboma of Optic Nerve |
| 120433 |
Coloboma, Uveal, with Cleft Lip and Palate and Mental Retardation |
| 303650 |
Colonic Atresia |
| 120440 |
Colonic Varices without Portal Hypertension |
| 303800 |
Colorblindness, Partial, Deutan Series; CBD |
| 303900 |
Colorblindness, Partial, Protan Series; CBP |
| 114500 |
Colorectal Cancer; CRC (7 mouse models) |
| 609310 |
Colorectal Cancer, Hereditary Nonpolyposis, Type 2; HNPCC2 (2 mouse models) |
| 614337 |
Colorectal Cancer, Hereditary Nonpolyposis, Type 4; HNPCC4 |
| 614350 |
Colorectal Cancer, Hereditary Nonpolyposis, Type 5; HNPCC5 |
| 614331 |
Colorectal Cancer, Hereditary Nonpolyposis, Type 6; HNPCC6 |
| 614385 |
Colorectal Cancer, Hereditary Nonpolyposis, Type 7; HNPCC7 |
| 613244 |
Colorectal Cancer, Hereditary Nonpolyposis, Type 8; HNPCC8 |
| 612591 |
Colorectal Cancer, Susceptibility to, 10; CRCS10 |
| 612592 |
Colorectal Cancer, Susceptibility to, 11; CRCS11 |
| 615083 |
Colorectal Cancer, Susceptibility to, 12; CRCS12 |
| 608812 |
Colorectal Cancer, Susceptibility to, 1; CRCS1 |
| 611469 |
Colorectal Cancer, Susceptibility to, 2; CRCS2 |
| 612229 |
Colorectal Cancer, Susceptibility to, 3; CRCS3 |
| 612230 |
Colorectal Cancer, Susceptibility to, 5; CRCS5 |
| 612231 |
Colorectal Cancer, Susceptibility to, 6; CRCS6 |
| 612232 |
Colorectal Cancer, Susceptibility to, 7; CRCS7 |
| 612589 |
Colorectal Cancer, Susceptibility to, 8; CRCS8 |
| 612590 |
Colorectal Cancer, Susceptibility to, 9; CRCS9 |
| 233650 |
Combined Cellular and Humoral Immune Defects with Granulomas; CCHIDG |
| 312863 |
Combined Immunodeficiency, X-Linked; CIDX |
| 216920 |
Combined Inflammatory and Immunologic Defect |
| 614265 |
Combined Malonic and Methylmalonic Aciduria; CMAMMA |
| 614702 |
Combined Oxidative Phosphorylation Deficiency 10; COXPD10 |
| 614922 |
Combined Oxidative Phosphorylation Deficiency 11; COXPD11 |
| 614924 |
Combined Oxidative Phosphorylation Deficiency 12; COXPD12 |
| 614932 |
Combined Oxidative Phosphorylation Deficiency 13; COXPD13 |
| 614946 |
Combined Oxidative Phosphorylation Deficiency 14; COXPD14 |
| 614947 |
Combined Oxidative Phosphorylation Deficiency 15; COXPD15 |
| 609060 |
Combined Oxidative Phosphorylation Deficiency 1; COXPD1 |
| 610498 |
Combined Oxidative Phosphorylation Deficiency 2; COXPD2 |
| 610505 |
Combined Oxidative Phosphorylation Deficiency 3; COXPD3 |
| 610678 |
Combined Oxidative Phosphorylation Deficiency 4; COXPD4 |
| 611719 |
Combined Oxidative Phosphorylation Deficiency 5; COXPD5 |
| 300816 |
Combined Oxidative Phosphorylation Deficiency 6; COXPD6 |
| 613559 |
Combined Oxidative Phosphorylation Deficiency 7; COXPD7 |
| 614096 |
Combined Oxidative Phosphorylation Deficiency 8; COXPD8 |
| 614582 |
Combined Oxidative Phosphorylation Deficiency 9; COXPD9 |
| 611721 |
Combined Saposin Deficiency |
| 120450 |
Comedones, Familial Dyskeratotic |
| 120500 |
Commissural Lip Pits |
| 217000 |
Complement Component 2 Deficiency; C2D |
| 613779 |
Complement Component 3 Deficiency, Autosomal Recessive; C3D |
| 614380 |
Complement Component 4a Deficiency; C4AD |
| 614379 |
Complement Component 4b Deficiency; C4BD |
| 120790 |
Complement Component 4, Partial Deficiency of |
| 609536 |
Complement Component 5 Deficiency; C5D |
| 612446 |
Complement Component 6 Deficiency; C6D |
| 610102 |
Complement Component 7 Deficiency; C7D |
| 613790 |
Complement Component 8 Deficiency, Type I; C8D1 |
| 613789 |
Complement Component 8 Deficiency, Type II; C8D2 |
| 613825 |
Complement Component 9 Deficiency; C9D |
| 216950 |
Complement Component C1r/C1s Deficiency |
| 613783 |
Complement Component C1s Deficiency; C1SD |
| 138470 |
Complement Factor B; CFB |
| 613912 |
Complement Factor D Deficiency; CFDD |
| 609814 |
Complement Factor H Deficiency; CFHD |
| 610984 |
Complement Factor I Deficiency; CFID |
| 602093 |
Cone Dystrophy 3; COD3 (3 mouse models) |
| 613093 |
Cone Dystrophy 4; COD4 |
| 304030 |
Cone Dystrophy, X-Linked, with Tapetal-Like Sheen |
| 610283 |
Cone-Rod Dystrophy 10; CORD10 |
| 610381 |
Cone-Rod Dystrophy 11; CORD11 |
| 612657 |
Cone-Rod Dystrophy 12; CORD12 |
| 608194 |
Cone-Rod Dystrophy 13; CORD13 |
| 613660 |
Cone-Rod Dystrophy 15; CORD15 |
| 614500 |
Cone-Rod Dystrophy 16; CORD16 |
| 600624 |
Cone-Rod Dystrophy 1; CORD1 |
| 120970 |
Cone-Rod Dystrophy 2; CORD2 |
| 604116 |
Cone-Rod Dystrophy 3; CORD3 (2 mouse models) |
| 600977 |
Cone-Rod Dystrophy 5; CORD5 |
| 601777 |
Cone-Rod Dystrophy 6; CORD6 (1 mouse model) |
| 603649 |
Cone-Rod Dystrophy 7; CORD7 |
| 605549 |
Cone-Rod Dystrophy 8; CORD8 |
| 612775 |
Cone-Rod Dystrophy 9; CORD9 |
| 304020 |
Cone-Rod Dystrophy, X-Linked, 1; CORDX1 (2 mouse models) |
| 300085 |
Cone-Rod Dystrophy, X-Linked, 2; CORDX2 |
| 300476 |
Cone-Rod Dystrophy, X-Linked, 3; CORDX3 |
| 604168 |
Congenital Cataracts, Facial Dysmorphism, and Neuropathy |
| 614482 |
Congenital Cataracts, Hearing Loss, and Neurodegeneration; CCHLND |
| 608484 |
Congenital Corneal Opacities, Cornea Guttata, and Corectopia |
| 212065 |
Congenital Disorder of Glycosylation, Type IA; CDG1A |
| 602579 |
Congenital Disorder of Glycosylation, Type IB; CDG1B |
| 603147 |
Congenital Disorder of Glycosylation, Type Ic; CDG1C |
| 601110 |
Congenital Disorder of Glycosylation, Type ID; CDG1D |
| 608799 |
Congenital Disorder of Glycosylation, Type IE; CDG1E |
| 609180 |
Congenital Disorder of Glycosylation, Type IF; CDG1F |
| 607143 |
Congenital Disorder of Glycosylation, Type IG; CDG1G |
| 608104 |
Congenital Disorder of Glycosylation, Type IH; CDG1H |
| 212066 |
Congenital Disorder of Glycosylation, Type IIA; CDG2A (2 mouse models) |
| 606056 |
Congenital Disorder of Glycosylation, Type IIB; CDG2B |
| 266265 |
Congenital Disorder of Glycosylation, Type IIC; CDG2C (1 mouse model) |
| 607906 |
Congenital Disorder of Glycosylation, Type II; CDG1I |
| 607091 |
Congenital Disorder of Glycosylation, Type Iid; CDG2D |
| 608779 |
Congenital Disorder of Glycosylation, Type Iie; CDG2E |
| 603585 |
Congenital Disorder of Glycosylation, Type Iif; CDG2F |
| 611209 |
Congenital Disorder of Glycosylation, Type Iig; CDG2G |
| 611182 |
Congenital Disorder of Glycosylation, Type Iih; CDG2H |
| 613612 |
Congenital Disorder of Glycosylation, Type III; CDG2I |
| 212067 |
Congenital Disorder of Glycosylation, Type I/IIX |
| 613489 |
Congenital Disorder of Glycosylation, Type Iij; CDG2J |
| 614727 |
Congenital Disorder of Glycosylation, Type Iik; CDG2K |
| 614576 |
Congenital Disorder of Glycosylation, Type Iil; CDG2L |
| 608093 |
Congenital Disorder of Glycosylation, Type IJ; CDG1J |
| 608540 |
Congenital Disorder of Glycosylation, Type IK; CDG1K |
| 608776 |
Congenital Disorder of Glycosylation, Type IL: Cdg1l |
| 610768 |
Congenital Disorder of Glycosylation, Type Im; CDG1M |
| 612015 |
Congenital Disorder of Glycosylation, Type In; CDG1N |
| 612937 |
Congenital Disorder of Glycosylation, Type Io; CDG1O |
| 613661 |
Congenital Disorder of Glycosylation, Type Ip; CDG1P |
| 612379 |
Congenital Disorder of Glycosylation, Type Iq; CDG1Q |
| 614507 |
Congenital Disorder of Glycosylation, Type Ir; CDG1R |
| 300884 |
Congenital Disorder of Glycosylation, Type Is; CDG1S |
| 614921 |
Congenital Disorder of Glycosylation, Type It; CDG1T |
| 615042 |
Congenital Disorder of Glycosylation, Type Iu; CDG1U |
| 217085 |
Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly |
| 614954 |
Congenital Heart Defects, Multiple Types, 3; CHTD3 |
| 614980 |
Congenital Heart Disease, Multiple Types, 2; CHTD2 |
| 308050 |
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects |
| 612918 |
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi |
| 217095 |
Conotruncal Heart Malformations; CTHM (3 mouse models) |
| 217100 |
Constricting Bands, Congenital |
| 217150 |
Contractures, Congenital, Torticollis, and Malignant Hyperthermia |
| 602066 |
Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis; |
| 217200 |
Convulsive Disorder, Familial, with Prenatal or Early Onset |
| 121270 |
Copper Deficiency, Familial Benign |
| 121300 |
Coproporphyria, Hereditary; HCP |
| 608158 |
CoQ-Responsive Oxphos Deficiency |
| 121350 |
Coracoclavicular Joint, Anomalous |
| 121390 |
Cornea Guttata with Anterior Polar Cataracts |
| 217520 |
Corneal Degeneration, Band-Shaped Spheroid |
| 121450 |
Corneal Degeneration, Ribbonlike, with Deafness |
| 217400 |
Corneal Dystrophy and Perceptive Deafness; CDPD |
| 607541 |
Corneal Dystrophy, Avellino Type; CDA |
| 217500 |
Corneal Dystrophy, Band-Shaped |
| 610048 |
Corneal Dystrophy, Congenital Stromal; CSCD (1 mouse model) |
| 300779 |
Corneal Dystrophy, Endothelial, X-Linked; XECD |
| 121820 |
Corneal Dystrophy, Epithelial Basement Membrane; EBMD |
| 121850 |
Corneal Dystrophy, Fleck |
| 136800 |
Corneal Dystrophy, Fuchs Endothelial, 1; FECD1 (1 mouse model) |
| 610158 |
Corneal Dystrophy, Fuchs Endothelial, 2; FECD2 |
| 613267 |
Corneal Dystrophy, Fuchs Endothelial, 3; FECD3 |
| 613268 |
Corneal Dystrophy, Fuchs Endothelial, 4; FECD4 |
| 613269 |
Corneal Dystrophy, Fuchs Endothelial, 5; FECD5 |
| 613270 |
Corneal Dystrophy, Fuchs Endothelial, 6; FECD6 |
| 613271 |
Corneal Dystrophy, Fuchs Endothelial, 7; FECD7 |
| 204870 |
Corneal Dystrophy, Gelatinous Drop-Like; GDLD |
| 121900 |
Corneal Dystrophy, Groenouw Type I; CDGG1 |
| 608471 |
Corneal Dystrophy, Lattice Type IIIA; CDL3A |
| 122200 |
Corneal Dystrophy, Lattice Type I; LCD1 |
| 300778 |
Corneal Dystrophy, Lisch Epithelial; LECD |
| 122100 |
Corneal Dystrophy, Meesmann; MECD |
| 608470 |
Corneal Dystrophy of Bowman Layer, Type I; CDB1 |
| 602082 |
Corneal Dystrophy of Bowman Layer, Type II; CDB2 |
| 612868 |
Corneal Dystrophy, Posterior Amorphous; PACD |
| 122000 |
Corneal Dystrophy, Posterior Polymorphous, 1; PPCD1 (2 mouse models) |
| 609140 |
Corneal Dystrophy, Posterior Polymorphous, 2; PPCD2 |
| 609141 |
Corneal Dystrophy, Posterior Polymorphous, 3; PPCD3 (2 mouse models) |
| 612867 |
Corneal Dystrophy, Subepithelial Mucinous; SMCD |
| 121700 |
Corneal Endothelial Dystrophy 1, Autosomal Dominant; CHED1 |
| 217700 |
Corneal Endothelial Dystrophy 2, Autosomal Recessive; CHED2 |
| 122450 |
Corneal Hypesthesia, Familial |
| 122430 |
Corneal Hypesthesia with Retinal Abnormalities, Sensorineural Deafness, Unusual Facies, Persistent Ductus Arteriosus, and Mental Retardation |
| 121400 |
Cornea Plana 1; CNA1 |
| 217300 |
Cornea Plana 2; CNA2 (1 mouse model) |
| 122470 |
Cornelia De Lange Syndrome 1; CDLS1 (1 mouse model) |
| 300590 |
Cornelia De Lange Syndrome 2; CDLS2 |
| 610759 |
Cornelia De Lange Syndrome 3; CDLS3 |
| 614701 |
Cornelia De Lange Syndrome 4; CDLS4 |
| 300882 |
Cornelia De Lange Syndrome 5; CDLS5 |
| 122440 |
Corneodermatoosseous Syndrome |
| 608320 |
Coronary Artery Disease, Autosomal Dominant, 1; ADCAD1 |
| 610947 |
Coronary Artery Disease, Autosomal Dominant 2; ADCAD2 |
| 122455 |
Coronary Artery Dissection, Spontaneous |
| 607339 |
Coronary Heart Disease, Susceptibility to, 1 |
| 608316 |
Coronary Heart Disease, Susceptibility to, 2 |
| 300464 |
Coronary Heart Disease, Susceptibility to, 3 |
| 608318 |
Coronary Heart Disease, Susceptibility to, 4 |
| 608901 |
Coronary Heart Disease, Susceptibility to, 5 |
| 614466 |
Coronary Heart Disease, Susceptibility to, 6; CHDS6 |
| 610938 |
Coronary Heart Disease, Susceptibility to, 7; CHDS7 |
| 611139 |
Coronary Heart Disease, Susceptibility to, 8; CHDS8 |
| 612030 |
Coronary Heart Disease, Susceptibility to, 9; CHDS9 |
| 217990 |
Corpus Callosum, Agenesis of |
| 300004 |
Corpus Callosum, Agenesis of, with Abnormal Genitalia |
| 217980 |
Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence |
| 300472 |
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia |
| 304100 |
Corpus Callosum, Partial Agenesis of, X-Linked |
| 218010 |
Cortical Blindness, Retardation, and Postaxial Polydactyly |
| 604922 |
Cortical Defects, Wormian Bones, and Dentinogenesis Imperfecta |
| 614039 |
Cortical Dysplasia, Complex, with Other Brain Malformations; CDCBM |
| 610042 |
Cortical Dysplasia-Focal Epilepsy Syndrome (1 mouse model) |
| 614115 |
Cortical Malformations, Occipital; OCCM |
| 611489 |
Corticosteroid-Binding Globulin Deficiency (1 mouse model) |
| 203400 |
Corticosterone Methyloxidase Type I Deficiency |
| 610600 |
Corticosterone Methyloxidase Type II Deficiency |
| 604931 |
Cortisone Reductase Deficiency 1; CORTRD1 |
| 614662 |
Cortisone Reductase Deficiency 2; CORTRD2 (1 mouse model) |
| 218040 |
Costello Syndrome (1 mouse model) |
| 122580 |
Costocoracoid Ligament, Congenitally Short |
| 122700 |
Coumarin Resistance |
| 260660 |
Cousin Syndrome |
| 310490 |
Cowchock Syndrome; COWCK |
| 158350 |
Cowden Syndrome 1; CWS1 (10 mouse models) |
| 612359 |
Cowden Syndrome 2; CWS2 |
| 615106 |
Cowden Syndrome 3; CWS3 |
| 615107 |
Cowden Syndrome 4; CWS4 |
| 615108 |
Cowden Syndrome 5; CWS5 |
| 615109 |
Cowden Syndrome 6; CWS6 |
| 122750 |
Coxa Vara |
| 122780 |
Coxoauricular Syndrome |
| 120050 |
Coxsackievirus B3 Susceptibility; CXB3S |
| 218050 |
Cramps, Familial Adolescent |
| 218090 |
Crane-Heise Syndrome |
| 218100 |
Cranial Nerves, Congenital Paresis of |
| 218200 |
Cranial Nerves, Recurrent Paresis of |
| 122850 |
Cranioacrofacial Syndrome |
| 122860 |
Craniodiaphyseal Dysplasia, Autosomal Dominant; CDD |
| 218300 |
Craniodiaphyseal Dysplasia; CDD |
| 218330 |
Cranioectodermal Dysplasia 1; CED1 |
| 613610 |
Cranioectodermal Dysplasia 2; CED2 |
| 614099 |
Cranioectodermal Dysplasia 3; CED3 |
| 614378 |
Cranioectodermal Dysplasia 4; CED4 |
| 608227 |
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation |
| 614195 |
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome; CAASDS |
| 122880 |
Craniofacial-Deafness-Hand Syndrome; CDHS |
| 614132 |
Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome; CFSMR |
| 218340 |
Craniofacial Dysmorphism with Ocular Coloboma, Absent Corpus Callosum, and Aortic Dilatation |
| 122900 |
Craniofacial Dysostosis with Diaphyseal Hyperplasia |
| 218350 |
Craniofacial Dyssynostosis with Short Stature |
| 601707 |
Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development |
| 114620 |
Craniofaciofrontodigital Syndrome |
| 300712 |
Craniofacioskeletal Syndrome |
| 304110 |
Craniofrontonasal Syndrome; CFNS (1 mouse model) |
| 607812 |
Craniolenticulosutural Dysplasia; CLSD |
| 615118 |
Craniometadiaphyseal Dysplasia; CRMDD |
| 123000 |
Craniometaphyseal Dysplasia, Autosomal Dominant; CMDD (1 mouse model) |
| 218400 |
Craniometaphyseal Dysplasia, Autosomal Recessive; CMDR |
| 602558 |
Craniomicromelic Syndrome |
| 123050 |
Craniorhiny |
| 218450 |
Craniostenosis, Sagittal, with Congenital Heart Disease, Mental Deficiency, and Mandibular Ankylosis |
| 600593 |
Craniosynostosis, Adelaide Type; CRSA |
| 614188 |
Craniosynostosis and Dental Anomalies; CRSDA |
| 608432 |
Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism |
| 218650 |
Craniosynostosis-Mental Retardation-Clefting Syndrome |
| 218649 |
Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig |
| 601222 |
Craniosynostosis, Philadelphia Type |
| 606529 |
Craniosynostosis Syndrome, Autosomal Recessive |
| 123100 |
Craniosynostosis, Type 1; CRS1 (1 mouse model) |
| 604757 |
Craniosynostosis, Type 2; CRS2 (4 mouse models) |
| 218530 |
Craniosynostosis with Anomalies of the Cranial Base and Digits |
| 603595 |
Craniosynostosis with Ectopia Lentis |
| 218550 |
Craniosynostosis with Fibular Aplasia |
| 608279 |
Craniosynostosis with Ocular Abnormalities and Hallucal Defects |
| 218670 |
Craniotelencephalic Dysplasia |
| 602472 |
Creases, Infra-Auricular Cutaneous, with Tall Stature and Advanced Bone Age |
| 300352 |
Creatine Deficiency Syndrome, X-Linked (2 mouse models) |
| 123320 |
Creatine Phosphokinase, Elevated Serum |
| 606851 |
Cree Mental Retardation Syndrome |
| 123400 |
Creutzfeldt-Jakob Disease; CJD (7 mouse models) |
| 123450 |
Cri-Du-Chat Syndrome |
| 218800 |
Crigler-Najjar Syndrome, Type I (2 mouse models) |
| 606785 |
Crigler-Najjar Syndrome, Type II |
| 218900 |
Crome Syndrome |
| 123500 |
Crouzon Syndrome (5 mouse models) |
| 612247 |
Crouzon Syndrome with Acanthosis Nigricans; CAN |
| 605945 |
Crumpled Helices and Small Mouth |
| 123540 |
Cryofibrinogenemia, Familial Primary |
| 123550 |
Cryoglobulinemia, Familial Mixed |
| 608885 |
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly |
| 123560 |
Cryptomicrotia-Brachydactyly Syndrome |
| 123570 |
Cryptophthalmos, Unilateral or Bilateral, Isolated |
| 219050 |
Cryptorchidism, Unilateral or Bilateral (5 mouse models) |
| 123557 |
Cryptotia, Familial |
| 123580 |
Crystallin, Alpha-A; CRYAA (9 mouse models) |
| 600929 |
Crystallin, Beta-B1; CRYBB1 |
| 123620 |
Crystallin, Beta-B2; CRYBB2 |
| 123680 |
Crystallin, Gamma-C; CRYGC (1 mouse model) |
| 123690 |
Crystallin, Gamma-D; CRYGD |
| 123730 |
Crystallin, Gamma-S; CRYGS |
| 211750 |
C Syndrome |
| 300471 |
Cubitus Valgus with Mental Retardation and Unusual Facies |
| 607656 |
Curly Hair-Acral Keratoderma-Caries Syndrome |
| 176450 |
Currarino Syndrome |
| 219070 |
Curved Nail of Fourth Toe |
| 248910 |
Cutaneous Mastocytosis, Conductive Hearing Loss and Microtia |
| 219095 |
Cutaneous Photosensitivity and Colitis, Lethal |
| 614564 |
Cutaneous Telangiectasia and Cancer Syndrome, Familial; FCTCS |
| 123700 |
Cutis Laxa, Autosomal Dominant 1; ADCL1 (2 mouse models) |
| 614434 |
Cutis Laxa, Autosomal Dominant 2; ADCL2 |
| 219100 |
Cutis Laxa, Autosomal Recessive, Type IA; ARCL1A (2 mouse models) |
| 614437 |
Cutis Laxa, Autosomal Recessive, Type IB; ARCL1B |
| 613177 |
Cutis Laxa, Autosomal Recessive, Type Ic; ARCL1C |
| 219200 |
Cutis Laxa, Autosomal Recessive, Type IIA; ARCL2A |
| 612940 |
Cutis Laxa, Autosomal Recessive, Type IIB; ARCL2B |
| 219150 |
Cutis Laxa, Autosomal Recessive, Type IIIA; ARCL3A |
| 614438 |
Cutis Laxa, Autosomal Recessive, Type Iiib; ARCL3B |
| 614100 |
Cutis Laxa, Neonatal, with Marfanoid Phenotype |
| 219250 |
Cutis Marmorata Telangiectatica Congenita; CMTC |
| 219300 |
Cutis Verticis Gyrata and Mental Retardation; CVG/MR |
| 605685 |
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness |
| 304200 |
Cutis Verticis Gyrata, Thyroid Aplasia, and Mental Retardation |
| 304300 |
Cyanide, Inability to Smell |
| 219400 |
Cyanosis and Hepatic Disease |
| 613977 |
Cyanosis, Transient Neonatal; TNCY |
| 162800 |
Cyclic Neutropenia |
| 500007 |
Cyclic Vomiting Syndrome; CVS |
| 132700 |
Cylindromatosis, Familial |
| 123853 |
Cyprus Facial Neuromusculoskeletal Syndrome |
| 219500 |
Cystathioninuria (1 mouse model) |
| 219550 |
Cysteine Peptiduria |
| 123880 |
Cystic Angiomatosis of Bone, Diffuse |
| 219600 |
Cystic Disease of Lung |
| 219700 |
Cystic Fibrosis; CF (19 mouse models) |
| 603855 |
Cystic Fibrosis, Modifier of, 1; CFM1 |
| 219721 |
Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Subnormal Mentality |
| 219750 |
Cystinosis, Adult Nonnephropathic |
| 219900 |
Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type |
| 219800 |
Cystinosis, Nephropathic; CTNS (1 mouse model) |
| 220100 |
Cystinuria (4 mouse models) |
| 608508 |
Cytochrome B(-245), Alpha Subunit; CYBA |
| 122720 |
Cytochrome P450, Subfamily IIA, Polypeptide 6; CYP2A6 |
| 601129 |
Cytochrome P450, Subfamily IIC, Polypeptide 8; CYP2C8 |
| 124060 |
Cytochrome P450, Subfamily I, Polypeptide 2; CYP1A2 |
| 123890 |
Cytotoxic T Lymphocyte-Associated 4; CTLA4 |
| 609162 |
Czech Dysplasia |
Analysis Tools