| OMIM ID |
Human Disease |
| 600721 |
D-2-hydroxyglutaric Aciduria 1 |
| 613657 |
D-2-hydroxyglutaric Aciduria 2 |
| 220210 |
Dandy-Walker-Like Malformation with Atrioventricular Septal Defect |
| 304340 |
Dandy-Walker Malformation with Mental Retardation, Basal Ganglia Disease, and Seizures |
| 220219 |
Dandy-Walker Malformation with Mental Retardation, Macrocephaly, Myopia, and Brachytelephalangy |
| 609222 |
Dandy-Walker Malformation with Occipital Cephalocele, Autosomal Dominant; |
| 220220 |
Dandy-Walker Malformation with Postaxial Polydactyly |
| 220200 |
Dandy-Walker Syndrome; DWS (3 mouse models) |
| 300257 |
Danon Disease (1 mouse model) |
| 124100 |
Danubian Endemic Familial Nephropathy |
| 124200 |
Darier-White Disease; DAR (1 mouse model) |
| 124300 |
Darwinian Tubercle of Pinna |
| 124400 |
Darwinian Tubercle of Pinna |
| 611733 |
Dauwerse-Peters Syndrome |
| 261515 |
D-Bifunctional Protein Deficiency (2 mouse models) |
| 580000 |
Deafness, Aminoglycoside-Induced |
| 601316 |
Deafness, Autosomal Dominant 10; DFNA10 |
| 601317 |
Deafness, Autosomal Dominant 11; DFNA11 |
| 601543 |
Deafness, Autosomal Dominant 12; DFNA12 (1 mouse model) |
| 601868 |
Deafness, Autosomal Dominant 13; DFNA13 (1 mouse model) |
| 602459 |
Deafness, Autosomal Dominant 15; DFNA15 |
| 603964 |
Deafness, Autosomal Dominant 16; DFNA16 |
| 603622 |
Deafness, Autosomal Dominant 17; DFNA17 |
| 606012 |
Deafness, Autosomal Dominant 18; DFNA18 |
| 124900 |
Deafness, Autosomal Dominant 1; DFNA1 |
| 604717 |
Deafness, Autosomal Dominant 20; DFNA20 |
| 607017 |
Deafness, Autosomal Dominant 21; DFNA21 |
| 606346 |
Deafness, Autosomal Dominant 22; DFNA22 (1 mouse model) |
| 605192 |
Deafness, Autosomal Dominant 23; DFNA23 |
| 606282 |
Deafness, Autosomal Dominant 24; DFNA24 |
| 605583 |
Deafness, Autosomal Dominant 25; DFNA25 (2 mouse models) |
| 612431 |
Deafness, Autosomal Dominant 27; DFNA27 |
| 608641 |
Deafness, Autosomal Dominant 28; DFNA28 |
| 600101 |
Deafness, Autosomal Dominant 2A; DFNA2A |
| 612644 |
Deafness, Autosomal Dominant 2B; DFNA2B |
| 606451 |
Deafness, Autosomal Dominant 30; DFNA30 |
| 608645 |
Deafness, Autosomal Dominant 31; DFNA31 |
| 614211 |
Deafness, Autosomal Dominant 33; DFNA33 |
| 606705 |
Deafness, Autosomal Dominant 36; DFNA36 (3 mouse models) |
| 605594 |
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 |
| 601544 |
Deafness, Autosomal Dominant 3A; DFNA3A |
| 612643 |
Deafness, Autosomal Dominant 3b; DFNA3B |
| 608224 |
Deafness, Autosomal Dominant 41; DFNA41 |
| 608394 |
Deafness, Autosomal Dominant 43; DFNA43 |
| 607453 |
Deafness, Autosomal Dominant 44; DFNA44 |
| 608652 |
Deafness, Autosomal Dominant 47; DFNA47 |
| 607841 |
Deafness, Autosomal Dominant 48; DFNA48 |
| 608372 |
Deafness, Autosomal Dominant 49; DFNA49 |
| 600652 |
Deafness, Autosomal Dominant 4A; DFNA4A (1 mouse model) |
| 614614 |
Deafness, Autosomal Dominant 4b; DFNA4B |
| 613074 |
Deafness, Autosomal Dominant 50; DFNA50 |
| 613558 |
Deafness, Autosomal Dominant 51; DFNA51 |
| 607683 |
Deafness, Autosomal Dominant 52; DFNA52 |
| 609965 |
Deafness, Autosomal Dominant 53; DFNA53 |
| 612642 |
Deafness, Autosomal Dominant 59; DFNA59 |
| 600994 |
Deafness, Autosomal Dominant 5; DFNA5 |
| 614152 |
Deafness, Autosomal Dominant 64; DFNA64 |
| 600965 |
Deafness, Autosomal Dominant 6; DFNA6 |
| 601412 |
Deafness, Autosomal Dominant 7; DFNA7 |
| 601369 |
Deafness, Autosomal Dominant 9; DFNA9 (1 mouse model) |
| 607197 |
Deafness, Autosomal Recessive |
| 601386 |
Deafness, Autosomal Recessive 12; DFNB12 (3 mouse models) |
| 603098 |
Deafness, Autosomal Recessive 13; DFNB13 |
| 603678 |
Deafness, Autosomal Recessive 14; DFNB14 |
| 601869 |
Deafness, Autosomal Recessive 15; DFNB15 |
| 603720 |
Deafness, Autosomal Recessive 16; DFNB16 (1 mouse model) |
| 603010 |
Deafness, Autosomal Recessive 17; DFNB17 |
| 602092 |
Deafness, Autosomal Recessive 18a; DFNB18A (2 mouse models) |
| 614945 |
Deafness, Autosomal Recessive 18b; DFNB18B |
| 220290 |
Deafness, Autosomal Recessive 1A; DFNB1A (3 mouse models) |
| 612645 |
Deafness, Autosomal Recessive 1B; DFNB1B |
| 604060 |
Deafness, Autosomal Recessive 20; DFNB20 |
| 603629 |
Deafness, Autosomal Recessive 21; DFNB21 |
| 607039 |
Deafness, Autosomal Recessive 22; DFNB22 (1 mouse model) |
| 609533 |
Deafness, Autosomal Recessive 23; DFNB23 |
| 611022 |
Deafness, Autosomal Recessive 24; DFNB24 |
| 613285 |
Deafness, Autosomal Recessive 25; DFNB25 |
| 605428 |
Deafness, Autosomal Recessive 26; DFNB26 |
| 605818 |
Deafness, Autosomal Recessive 27; DFNB27 |
| 609823 |
Deafness, Autosomal Recessive 28; DFNB28 |
| 614035 |
Deafness, Autosomal Recessive 29; DFNB29 (1 mouse model) |
| 600060 |
Deafness, Autosomal Recessive 2; DFNB2 |
| 607101 |
Deafness, Autosomal Recessive 30; DFNB30 (1 mouse model) |
| 607084 |
Deafness, Autosomal Recessive 31; DFNB31 (1 mouse model) |
| 608653 |
Deafness, Autosomal Recessive 32; DFNB32 |
| 607239 |
Deafness, Autosomal Recessive 33; DFNB33 |
| 608565 |
Deafness, Autosomal Recessive 35; DFNB35 |
| 609006 |
Deafness, Autosomal Recessive 36, with or without Vestibular Involvement; |
| 607821 |
Deafness, Autosomal Recessive 37; DFNB37 (1 mouse model) |
| 608219 |
Deafness, Autosomal Recessive 38; DFNB38 (2 mouse models) |
| 608265 |
Deafness, Autosomal Recessive 39; DFNB39 |
| 600316 |
Deafness, Autosomal Recessive 3; DFNB3 (1 mouse model) |
| 608264 |
Deafness, Autosomal Recessive 40; DFNB40 |
| 609646 |
Deafness, Autosomal Recessive 42; DFNB42 |
| 610154 |
Deafness, Autosomal Recessive 44; DFNB44 |
| 612433 |
Deafness, Autosomal Recessive 45; DFNB45 |
| 609647 |
Deafness, Autosomal Recessive 46; DFNB46 |
| 609946 |
Deafness, Autosomal Recessive 47; DFNB47 |
| 609439 |
Deafness, Autosomal Recessive 48; DFNB48 |
| 610153 |
Deafness, Autosomal Recessive 49; DFNB49 |
| 600791 |
Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct; (2 mouse models) |
| 609941 |
Deafness, Autosomal Recessive 51; DFNB51 |
| 609706 |
Deafness, Autosomal Recessive 53; DFNB53 |
| 609952 |
Deafness, Autosomal Recessive 55; DFNB55 |
| 610220 |
Deafness, Autosomal Recessive 59; DFNB59 (1 mouse model) |
| 600792 |
Deafness, Autosomal Recessive 5; DFNB5 |
| 613865 |
Deafness, Autosomal Recessive 61; DFNB61 |
| 610143 |
Deafness, Autosomal Recessive 62; DFNB62 |
| 611451 |
Deafness, Autosomal Recessive 63; DFNB63 (1 mouse model) |
| 610248 |
Deafness, Autosomal Recessive 65; DFNB65 |
| 610212 |
Deafness, Autosomal Recessive 66; DFNB66 |
| 610265 |
Deafness, Autosomal Recessive 67; DFNB67 |
| 610419 |
Deafness, Autosomal Recessive 68; DFNB68 |
| 600971 |
Deafness, Autosomal Recessive 6; DFNB6 |
| 614934 |
Deafness, Autosomal Recessive 70; DFNB70 |
| 612789 |
Deafness, Autosomal Recessive 71; DFNB71 |
| 613718 |
Deafness, Autosomal Recessive 74; DFNB74 |
| 613079 |
Deafness, Autosomal Recessive 77; DFNB77 |
| 613307 |
Deafness, Autosomal Recessive 79; DFNB79 |
| 600974 |
Deafness, Autosomal Recessive 7; DFNB7 (6 mouse models) |
| 614129 |
Deafness, Autosomal Recessive 81; DFNB81 |
| 613685 |
Deafness, Autosomal Recessive 83; DFNB83 |
| 613391 |
Deafness, Autosomal Recessive 84a; DFNB84A |
| 614944 |
Deafness, Autosomal Recessive 84b; DFNB84B |
| 613392 |
Deafness, Autosomal Recessive 85; DFNB85 |
| 614617 |
Deafness, Autosomal Recessive 86; DFNB86 |
| 613916 |
Deafness, Autosomal Recessive 89; DFNB89 |
| 601072 |
Deafness, Autosomal Recessive 8; DFNB8 |
| 613453 |
Deafness, Autosomal Recessive 91; DFNB91 |
| 614899 |
Deafness, Autosomal Recessive 93; DFNB93 |
| 614414 |
Deafness, Autosomal Recessive 96; DFNB96 |
| 614861 |
Deafness, Autosomal Recessive 98; DFNB98 |
| 601071 |
Deafness, Autosomal Recessive 9; DFNB9 (2 mouse models) |
| 300719 |
Deafness, Cataract, Retinitis Pigmentosa, and Sperm Abnormalities |
| 221200 |
Deafness, Cochlear, with Myopia and Intellectual Impairment |
| 124490 |
Deafness, Conductive Stapedial, with Ear Malformation and Facial Palsy |
| 221300 |
Deafness, Conductive, with Malformed External Ear |
| 221320 |
Deafness, Conductive, with Ptosis and Skeletal Anomalies |
| 220300 |
Deafness, Congenital, and Familial Myoclonic Epilepsy |
| 124480 |
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant; DDOD |
| 610706 |
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia |
| 124500 |
Deafness, Congenital, with Keratopachydermia and Constrictions of Fingers and Toes |
| 220900 |
Deafness, Congenital, with Total Albinism |
| 221350 |
Deafness, Congenital, with Vitiligo and Achalasia |
| 125230 |
Deafness-Craniofacial Syndrome |
| 304590 |
Deafness, High-Frequency Sensorineural, X-Linked |
| 304350 |
Deafness-Hypogonadism Syndrome; DHS |
| 124700 |
Deafness, Mid-Tone Neural |
| 221400 |
Deafness, Nerve Type, with Mesenteric Diverticula of Small Bowel and Progressive Sensory Neuropathy |
| 221500 |
Deafness, Neural, Congenital Moderate |
| 221700 |
Deafness, Neural, with Atypical Atopic Dermatitis |
| 605429 |
Deafness, Nonsyndromic, Modifier 1; DFNM1 |
| 500008 |
Deafness, Nonsyndromic Sensorineural, Mitochondrial |
| 221740 |
Deafness-Oligodontia Syndrome |
| 220500 |
Deafness, Onychodystrophy, Osteodystrophy, and Mental Retardation Syndrome |
| 601449 |
Deafness, Progressive, with Stapes Fixation |
| 611102 |
Deafness, Sensorineural, and Male Infertility |
| 221745 |
Deafness, Sensorineural, Autosomal-Mitochondrial Type |
| 124950 |
Deafness, Sensorineural, with Peripheral Neuropathy and Arterial Disease |
| 125000 |
Deafness, Unilateral |
| 612097 |
Deafness, Unilateral, with Delayed Endolymphatic Hydrops |
| 125050 |
Deafness with Anhidrotic Ectodermal Dysplasia |
| 304500 |
Deafness, X-Linked 1; DFNX1 |
| 304400 |
Deafness, X-Linked 2; DFNX2 (8 mouse models) |
| 300030 |
Deafness, X-Linked 3; DFNX3 |
| 300066 |
Deafness, X-Linked 4; DFNX4 |
| 300614 |
Deafness, X-Linked 5; DFNX5 |
| 400043 |
Deafness, Y-Linked 1; DFNY1 |
| 194380 |
Dehydrated Hereditary Stomatocytosis; DHS |
| 603528 |
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema |
| 147892 |
Deiodinase, Iodothyronine, Type I; DIO1 |
| 614163 |
Delayed Sleep Phase Syndrome, Susceptibility To; DSPS |
| 127750 |
Dementia, Lewy Body; DLB (2 mouse models) |
| 125320 |
Dementia/Parkinsonism with Non-Alzheimer Amyloid Plaques |
| 614172 |
Dendritic Cell, Monocyte, B Lymphocyte, and Natural Killer Lymphocyte Deficiency; DCML |
| 614371 |
Dengue Virus, Susceptibility to |
| 125280 |
Dens Evaginatus |
| 125300 |
Dens in Dente and Palatal Invaginations |
| 125370 |
Dentatorubral-Pallidoluysian Atrophy; DRPLA (5 mouse models) |
| 300009 |
Dent Disease 1 (2 mouse models) |
| 300555 |
Dent Disease 2 (2 mouse models) |
| 125400 |
Dentin Dysplasia, Type I; DTDP1 (1 mouse model) |
| 125420 |
Dentin Dysplasia, Type II (1 mouse model) |
| 125440 |
Dentin Dysplasia with Sclerotic Bones |
| 125490 |
Dentinogenesis Imperfecta 1; DGI1 |
| 125500 |
Dentinogenesis Imperfecta, Shields Type III (1 mouse model) |
| 194080 |
Denys-Drash Syndrome; DDS (6 mouse models) |
| 125460 |
Deoxyribose-5-Phosphate Aldolase Deficiency |
| 125530 |
Dermal Ridges, Nelson Syndrome |
| 125550 |
Dermal Ridges-Off-The-End; ROES |
| 125540 |
Dermal Ridges, Patternless |
| 603165 |
Dermatitis, Atopic (14 mouse models) |
| 605803 |
Dermatitis, Atopic, 2; ATOD2 |
| 605804 |
Dermatitis, Atopic, 3; ATOD3 |
| 605805 |
Dermatitis, Atopic, 4; ATOD4 |
| 605844 |
Dermatitis, Atopic, 5; ATOD5 |
| 605845 |
Dermatitis, Atopic, 6; ATOD6 |
| 613064 |
Dermatitis, Atopic, 7; ATOD7 |
| 613518 |
Dermatitis, Atopic, 8; ATOD8 |
| 613519 |
Dermatitis, Atopic, 9; ATOD9 |
| 601230 |
Dermatitis Herpetiformis, Familial |
| 607907 |
Dermatofibrosarcoma Protuberans; DFSP |
| 125570 |
Dermatoglyphics--Arch on Any Digit |
| 125590 |
Dermatoglyphics--Fingerprint Pattern |
| 125580 |
Dermatoglyphics--Finger Ridge Count |
| 221780 |
Dermatoglyphics--Hypothenar Radial Arch |
| 221760 |
Dermatoglyphics--Palmar Triradius D, Absence of |
| 221790 |
Dermatoleukodystrophy |
| 221810 |
Dermatoosteolysis, Kirghizian Type |
| 125595 |
Dermatopathia Pigmentosa Reticularis; DPR |
| 125600 |
Dermatosis Papulosa Nigra |
| 221800 |
Dermochondrocorneal Dystrophy |
| 125630 |
Dermodistortive Urticaria; DDU |
| 125635 |
Dermographism, Familial |
| 600679 |
Dermoid Cysts, Familial Frontonasal |
| 304730 |
Dermoids of Cornea; CND |
| 125640 |
Dermoodontodysplasia |
| 278800 |
De Sanctis-Cacchione Syndrome |
| 251450 |
Desbuquois Dysplasia; DBQD |
| 135290 |
Desmoid Disease, Hereditary |
| 602398 |
Desmosterolosis |
| 610136 |
Devriendt Syndrome |
| 221950 |
Dextrocardia with Unusual Facies and Microphthalmia |
| 220120 |
D-Glyceric Aciduria |
| 520000 |
Diabetes and Deafness, Maternally Inherited; MIDD |
| 125800 |
Diabetes Insipidus, Nephrogenic, Autosomal (8 mouse models) |
| 221995 |
Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification |
| 304800 |
Diabetes Insipidus, Nephrogenic, X-Linked (3 mouse models) |
| 125700 |
Diabetes Insipidus, Neurohypophyseal (2 mouse models) |
| 304900 |
Diabetes Insipidus, Neurohypophyseal Type |
| 605026 |
Diabetes Mellitus, Congenital Autoimmune |
| 601942 |
Diabetes Mellitus, Insulin-Dependent, 10; IDDM10 |
| 601208 |
Diabetes Mellitus, Insulin-Dependent, 11; IDDM11 |
| 601388 |
Diabetes Mellitus, Insulin-Dependent, 12; IDDM12 |
| 601318 |
Diabetes Mellitus, Insulin-Dependent, 13; IDDM13 |
| 601666 |
Diabetes Mellitus, Insulin-Dependent, 15; IDDM15 |
| 603266 |
Diabetes Mellitus, Insulin-Dependent, 17; IDDM17 |
| 605598 |
Diabetes Mellitus, Insulin-Dependent, 18; IDDM18 |
| 610155 |
Diabetes Mellitus, Insulin-Dependent, 19; IDDM19 |
| 125852 |
Diabetes Mellitus, Insulin-Dependent, 2 (2 mouse models) |
| 612520 |
Diabetes Mellitus, Insulin-Dependent, 20; IDDM20 |
| 612521 |
Diabetes Mellitus, Insulin-Dependent, 21; IDDM21 |
| 612522 |
Diabetes Mellitus, Insulin-Dependent, 22; IDDM22 |
| 612622 |
Diabetes Mellitus, Insulin-Dependent, 23; IDDM23 |
| 613006 |
Diabetes Mellitus, Insulin-Dependent, 24; IDDM24 |
| 600318 |
Diabetes Mellitus, Insulin-Dependent, 3; IDDM3 |
| 600319 |
Diabetes Mellitus, Insulin-Dependent, 4; IDDM4 |
| 600320 |
Diabetes Mellitus, Insulin-Dependent, 5; IDDM5 |
| 601941 |
Diabetes Mellitus, Insulin-Dependent, 6; IDDM6 |
| 600321 |
Diabetes Mellitus, Insulin-Dependent, 7; IDDM7 (1 mouse model) |
| 600883 |
Diabetes Mellitus, Insulin-Dependent, 8; IDDM8 |
| 222100 |
Diabetes Mellitus, Insulin-Dependent; IDDM (75 mouse models) |
| 300136 |
Diabetes Mellitus, Insulin-Dependent, X-Linked, Susceptibility to |
| 610549 |
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans |
| 612227 |
Diabetes Mellitus, Ketosis-Prone; KPD |
| 610199 |
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism (2 mouse models) |
| 601283 |
Diabetes Mellitus, Noninsulin-Dependent, 1; NIDDM1 |
| 601407 |
Diabetes Mellitus, Noninsulin-Dependent, 2; NIDDM2 |
| 603694 |
Diabetes Mellitus, Noninsulin-Dependent, 3 |
| 608036 |
Diabetes Mellitus, Noninsulin-Dependent, 4 |
| 125853 |
Diabetes Mellitus, Noninsulin-Dependent; NIDDM (34 mouse models) |
| 606176 |
Diabetes Mellitus, Permanent Neonatal; PNDM (4 mouse models) |
| 601410 |
Diabetes Mellitus, Transient Neonatal, 1 (1 mouse model) |
| 610374 |
Diabetes Mellitus, Transient Neonatal, 2 |
| 610582 |
Diabetes Mellitus, Transient Neonatal, 3 |
| 222350 |
Diaminopentanuria |
| 613309 |
Diamond-Blackfan Anemia 10; DBA10 |
| 614900 |
Diamond-Blackfan Anemia 11; DBA11 |
| 606129 |
Diamond-Blackfan Anemia 2; DBA2 |
| 610629 |
Diamond-Blackfan Anemia 3; DBA3 |
| 612527 |
Diamond-Blackfan Anemia 4; DBA4 |
| 612528 |
Diamond-Blackfan Anemia 5; DBA5 |
| 612561 |
Diamond-Blackfan Anemia 6; DBA6 |
| 612562 |
Diamond-Blackfan Anemia 7; DBA7 |
| 612563 |
Diamond-Blackfan Anemia 8; DBA8 |
| 613308 |
Diamond-Blackfan Anemia 9; DBA9 |
| 105650 |
Diamond-Blackfan Anemia; DBA (8 mouse models) |
| 606164 |
Diamond-Blackfan Anemia with Microtia and Cleft Palate |
| 605233 |
Dianzani Autoimmune Lymphoproliferative Disease |
| 608022 |
Diaphanospondylodysostosis |
| 601163 |
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects of Skull |
| 222400 |
Diaphragmatic Hernia 2; DIH2 (1 mouse model) |
| 610187 |
Diaphragmatic Hernia 3 |
| 142340 |
Diaphragmatic Hernia, Congenital (9 mouse models) |
| 112250 |
Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma; |
| 214700 |
Diarrhea 1, Secretory Chloride, Congenital; DIAR1 (1 mouse model) |
| 251850 |
Diarrhea 2, with Microvillus Atrophy; DIAR2 (1 mouse model) |
| 270420 |
Diarrhea 3, Secretory Sodium, Congenital; DIAR3 |
| 610370 |
Diarrhea 4, Malabsorptive, Congenital; DIAR4 |
| 613217 |
Diarrhea 5, with Tufting Enteropathy, Congenital; DIAR5 |
| 614616 |
Diarrhea 6; DIAR6 |
| 520100 |
Diarrhea, Chronic, with Villous Atrophy |
| 125890 |
Diarrhea, Glucose-Stimulated Secretory, with Common Variable Immunodeficiency |
| 612198 |
Diastasis Recti and Weakness of the Linea Alba |
| 125900 |
Diastema, Dental Medial |
| 222500 |
Diastematomyelia |
| 222600 |
Diastrophic Dysplasia (1 mouse model) |
| 222690 |
Dibasic Amino Aciduria I |
| 222730 |
Dicarboxylic Aminoaciduria (1 mouse model) |
| 188400 |
DiGeorge Syndrome; DGS (35 mouse models) |
| 601362 |
Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 |
| 606835 |
Digital Arthropathy-Brachydactyly, Familial; FDAB |
| 119900 |
Digital Clubbing, Isolated Congenital |
| 126050 |
Digitotalar Dysmorphism |
| 246900 |
Dihydrolipoamide Dehydrogenase Deficiency; DLDD |
| 222748 |
Dihydropyrimidinase Deficiency |
| 274270 |
Dihydropyrimidine Dehydrogenase Deficiency |
| 126070 |
Dilution, Pigmentary |
| 605850 |
Dimethylglycine Dehydrogenase Deficiency; DMGDHD |
| 126100 |
Dimples, Facial |
| 190340 |
Discoid Fibromas, Familial Multiple; FMDF |
| 126180 |
Discrimination, Two-Point, Reduction in |
| 603133 |
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation |
| 601450 |
Dislocation of Hip, Congenital, with Hyperextensibility of Fingers and Facial Dysmorphism |
| 613571 |
Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency |
| 223200 |
Disorganization, Mouse, Homolog of |
| 126190 |
Disproportionate Short Stature with Ptosis and Valvular Heart Lesions |
| 223300 |
Disseminated Sclerosis with Narcolepsy |
| 126250 |
Distal Osteosclerosis |
| 126300 |
Distichiasis |
| 126320 |
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature |
| 223330 |
Diverticulosis of Bowel, Hernia, and Retinal Detachment |
| 223320 |
Diverticulosis, Small-Intestinal |
| 223340 |
DK Phocomelia Syndrome |
| 126390 |
DNA, Low-Repetitive Sequences of |
| 126410 |
DNA, Satellite, Alpha Type |
| 126370 |
DNA, Satellite, III; HS3; D1Z1 |
| 223350 |
Dohle Bodies and Leukemia |
| 222448 |
Donnai-Barrow Syndrome (1 mouse model) |
| 246200 |
Donohue Syndrome |
| 223360 |
Dopamine Beta-Hydroxylase Deficiency, Congenital (1 mouse model) |
| 223380 |
Dopamine Beta-Hydroxylase, Plasma, Thermolability of |
| 126453 |
Dopamine Receptor D5; DRD5 |
| 126500 |
Double Nail for Fifth Toe |
| 126550 |
Doughnut Lesions of Skull, Familial |
| 179850 |
Dowling-Degos Disease; DDD |
| 190685 |
Down Syndrome (20 mouse models) |
| 126600 |
Doyne Honeycomb Retinal Dystrophy; DHRD (4 mouse models) |
| 607208 |
Dravet Syndrome (4 mouse models) |
| 609535 |
Drug Metabolism, Poor, Cyp2c19-Related |
| 608902 |
Drug Metabolism, Poor, Cyp2d6-Related |
| 607323 |
Duane-Radial Ray Syndrome; DRRS (4 mouse models) |
| 126800 |
Duane Retraction Syndrome 1; DURS1 |
| 604356 |
Duane Retraction Syndrome 2; DURS2 |
| 237500 |
Dubin-Johnson Syndrome; DJS (1 mouse model) |
| 223370 |
Dubowitz Syndrome |
| 223400 |
Duodenal Atresia |
| 126840 |
Duodenal Ulcer Due to Antral G-Cell Hyperfunction |
| 126850 |
Duodenal Ulcer, Hyperpepsinogenemic I |
| 606894 |
Duodenojejunal Atresia with Volvulus, Absent Dorsal Mesentery, and Absent Superior Mesenteric Artery |
| 126900 |
Dupuytren Contracture |
| 600771 |
Dwarfism, Familial, with Muscle Spasms |
| 127100 |
Dwarfism, Levi Type (1 mouse model) |
| 223500 |
Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone |
| 223540 |
Dwarfism, Mental Retardation, and Eye Abnormality |
| 223550 |
Dwarfism, Proportionate, with Hip Dislocation |
| 127200 |
Dwarfism with Stiff Joints and Ocular Abnormalities |
| 126950 |
Dwarfism with Tall Vertebrae |
| 223800 |
Dyggve-Melchior-Clausen Disease; DMC (1 mouse model) |
| 304950 |
Dyggve-Melchior-Clausen Syndrome, X-Linked |
| 224000 |
Dysautonomia-Like Disorder |
| 127350 |
Dyschondrosteosis and Nephritis |
| 127400 |
Dyschromatosis Symmetrica Hereditaria 1 |
| 127500 |
Dyschromatosis Universalis Hereditaria 1; DUH1 |
| 612715 |
Dyschromatosis Universalis Hereditaria 2; DUH2 |
| 603529 |
Dyserythropoiesis, Congenital, with Internuclear Chromatin Bridges and Ultrastructurally Normal Erythroblast Heterochromatin |
| 127550 |
Dyskeratosis Congenita, Autosomal Dominant, 1; DKCA1 (1 mouse model) |
| 613989 |
Dyskeratosis Congenita, Autosomal Dominant, 2; DKCA2 |
| 613990 |
Dyskeratosis Congenita, Autosomal Dominant, 3; DKCA3 |
| 224230 |
Dyskeratosis Congenita, Autosomal Recessive, 1; DKCB1 |
| 613987 |
Dyskeratosis Congenita, Autosomal Recessive, 2; DKCB2 |
| 613988 |
Dyskeratosis Congenita, Autosomal Recessive, 3; DKCB3 |
| 305000 |
Dyskeratosis Congenita, X-Linked; DKCX (2 mouse models) |
| 127600 |
Dyskeratosis, Hereditary Benign Intraepithelial |
| 606703 |
Dyskinesia, Familial, with Facial Myokymia; FDFM |
| 127700 |
Dyslexia, Susceptibility to, 1; DYX1 |
| 600202 |
Dyslexia, Susceptibility to, 2; DYX2 |
| 604254 |
Dyslexia, Susceptibility to, 3; DYX3 |
| 606896 |
Dyslexia, Susceptibility to, 5; DYX5 |
| 606616 |
Dyslexia, Susceptibility to, 6; DYX6 |
| 608995 |
Dyslexia, Susceptibility to, 8; DYX8 |
| 300509 |
Dyslexia, Susceptibility to, 9; DYX9 |
| 224250 |
Dysmyelination with Jaundice |
| 224300 |
Dysosteosclerosis |
| 600117 |
Dysphasia, Familial Developmental |
| 127800 |
Dysplasia Epiphysealis Hemimelica |
| 127820 |
Dysplasia Epiphysealis Hemimelica with Chondromas and Osteochondromas |
| 224400 |
Dyssegmental Dysplasia, Rolland-Desbuquois Type |
| 224410 |
Dyssegmental Dysplasia, Silverman-Handmaker Type; DDSH (2 mouse models) |
| 601561 |
Dyssegmental Dysplasia with Glaucoma |
| 128000 |
Dystelephalangy |
| 128235 |
Dystonia 12; DYT12 |
| 607671 |
Dystonia 13, Torsion, Autosomal Dominant; DYT13 |
| 607488 |
Dystonia 15, Myoclonic; DYT15 |
| 612067 |
Dystonia 16; DYT16 |
| 612406 |
Dystonia 17, Torsion, Autosomal Recessive; DYT17 |
| 128100 |
Dystonia 1, Torsion, Autosomal Dominant; DYT1 (4 mouse models) |
| 614588 |
Dystonia 21; DYT21 |
| 614860 |
Dystonia 23; DYT23 |
| 615034 |
Dystonia 24; DYT24 |
| 615073 |
Dystonia 25; DYT25 |
| 224500 |
Dystonia 2, Torsion, Autosomal Recessive; DYT2 |
| 314250 |
Dystonia 3, Torsion, X-Linked; DYT3 |
| 128101 |
Dystonia 4, Torsion, Autosomal Dominant; DYT4 |
| 602629 |
Dystonia 6, Torsion; DYT6 |
| 602124 |
Dystonia 7, Torsion; DYT7 |
| 601042 |
Dystonia 9; DYT9 |
| 128230 |
Dystonia, Dopa-Responsive; DRD (2 mouse models) |
| 612716 |
Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency (1 mouse model) |
| 611284 |
Dystonia, Focal, Task-Specific; FTSD |
| 607371 |
Dystonia, Juvenile-Onset |
| 611694 |
Dystonia with Cerebellar Atrophy; DYTCA |
| 224550 |
Dystonia with Ringbinden |
| 145680 |
Dystransthyretinemic Euthyroidal Hyperthyroxinemia |
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