| OMIM ID |
Human Disease |
| 128290 |
Ear Antitragus, Tag at Base of |
| 128300 |
Ear Exostoses |
| 128400 |
Ear Flare |
| 128500 |
Ear Folding |
| 128900 |
Earlobe Attachment, Attached Vs Unattached |
| 128950 |
Earlobe Crease |
| 128980 |
Earlobes, Thickened, with Conductive Deafness From Incudostapedial Abnormalities |
| 613601 |
Early Repolarization Associated with Ventricular Fibrillation |
| 605105 |
Early Response to Neural Induction Gene |
| 128600 |
Ear Malformation |
| 128710 |
Ear Pits, Posterior Helical |
| 129000 |
Earring Holes, Natural |
| 128800 |
Ear without Helix |
| 224700 |
Ebstein Anomaly (1 mouse model) |
| 603669 |
Eccrine Syringofibroadenomatosis with Eyelid Abnormalities |
| 129150 |
Echo Virus 11 Sensitivity; E11S |
| 129490 |
Ectodermal Dysplasia 10a, Hypohidrotic/Hair/Nail Type, Autosomal Dominant; |
| 224900 |
Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive; ECTD10B (2 mouse models) |
| 614940 |
Ectodermal Dysplasia 11a, Hypohidrotic/Hair/Tooth Type, Autosomal Dominant; ECTD11A |
| 614941 |
Ectodermal Dysplasia 11b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive; ECTD11B |
| 305100 |
Ectodermal Dysplasia 1, Hypohidrotic, X-Linked; XHED (2 mouse models) |
| 602032 |
Ectodermal Dysplasia 4, Hair/Nail Type; ECTD4 |
| 614927 |
Ectodermal Dysplasia 5, Hair/Nail Type; ECTD5 |
| 614928 |
Ectodermal Dysplasia 6, Hair/Nail Type; ECTD6 |
| 614929 |
Ectodermal Dysplasia 7, Hair/Nail Type; ECTD7 |
| 602401 |
Ectodermal Dysplasia 8, Hair/Tooth/Nail Type; ECTD8 |
| 614931 |
Ectodermal Dysplasia 9, Hair/Nail Type; ECTD9 |
| 224800 |
Ectodermal Dysplasia and Neurosensory Deafness |
| 300301 |
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema; OLEDAID |
| 612132 |
Ectodermal Dysplasia, Anhidrotic, with T-Cell Immunodeficiency, Autosomal Dominant |
| 601375 |
Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type |
| 225040 |
Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum |
| 225050 |
Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia |
| 300291 |
Ectodermal Dysplasia, Hypohidrotic, with Immune Deficiency |
| 609944 |
Ectodermal Dysplasia, Sensorineural Hearing Loss, and Distinctive Facial Features |
| 604536 |
Ectodermal Dysplasia/Skin Fragility Syndrome |
| 613573 |
Ectodermal Dysplasia-Syndactyly Syndrome 1; EDSS1 |
| 613576 |
Ectodermal Dysplasia-Syndactyly Syndrome 2; EDSS2 |
| 129540 |
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet |
| 129510 |
Ectodermal Dysplasia, Trichoodontoonychial Type |
| 129550 |
Ectodermal Dysplasia with Adrenal Cyst |
| 600906 |
Ectodermal Dysplasia with Mental Retardation and Syndactyly |
| 601345 |
Ectodermal Dysplasia with Natal Teeth, Turnpenny Type |
| 129600 |
Ectopia Lentis 1, Isolated, Autosomal Dominant; ECTOL1 |
| 225100 |
Ectopia Lentis 2, Isolated, Autosomal Recessive; ECTOL2 |
| 225200 |
Ectopia Lentis Et Pupillae |
| 601552 |
Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism |
| 129750 |
Ectopia Pupillae |
| 129810 |
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate |
| 129830 |
Ectrodactyly-Cleft Palate Syndrome |
| 129900 |
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 1; EEC1 |
| 604292 |
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3; EEC3 (3 mouse models) |
| 601348 |
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia |
| 225290 |
Ectrodactyly-Polydactyly |
| 129840 |
Edema, Familial Idiopathic, Prepubertal |
| 614303 |
Edict Syndrome; EDICT |
| 129850 |
Edinburgh Malformation Syndrome |
| 225280 |
EEM Syndrome |
| 614546 |
Efavirenz, Poor Metabolism of |
| 129905 |
Egasyn |
| 606408 |
Ehlers-Danlos-Like Syndrome Due to Tenascin-X Deficiency (1 mouse model) |
| 130090 |
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified |
| 225320 |
Ehlers-Danlos Syndrome, Autosomal Recessive, Cardiac Valvular Form |
| 608763 |
Ehlers-Danlos Syndrome, Beasley-Cohen Type |
| 601776 |
Ehlers-Danlos Syndrome, Musculocontractural Type |
| 130070 |
Ehlers-Danlos Syndrome, Progeroid Form (2 mouse models) |
| 130000 |
Ehlers-Danlos Syndrome, Type I (4 mouse models) |
| 130010 |
Ehlers-Danlos Syndrome, Type II (2 mouse models) |
| 130020 |
Ehlers-Danlos Syndrome, Type III |
| 130050 |
Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant (2 mouse models) |
| 305200 |
Ehlers-Danlos Syndrome, Type V |
| 225400 |
Ehlers-Danlos Syndrome, Type Vi; EDS6 (1 mouse model) |
| 130060 |
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant |
| 225410 |
Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive (1 mouse model) |
| 130080 |
Ehlers-Danlos Syndrome, Type VIII |
| 225310 |
Ehlers-Danlos Syndrome with Platelet Dysfunction From Fibronectin Abnormality |
| 614557 |
Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss; EDSKMH |
| 600002 |
Eiken Skeletal Dysplasia |
| 130100 |
Elastosis Perforans Serpiginosa; EPS |
| 130190 |
Electroencephalographic Pattern, Beta Frequency, Quantitative Trait Locus; EEGBQTL |
| 130200 |
Electroencephalographic Peculiarity: 14 and 6 Per Sec. Positive Spike Phenomenon |
| 130300 |
Electroencephalographic Peculiarity: Fronto-Precentral Beta Wave Groups |
| 130400 |
Electroencephalographic Peculiarity: Occipital Slow Beta Waves |
| 256710 |
Elejalde Disease (1 mouse model) |
| 611804 |
Elliptocytosis 1; EL1 (1 mouse model) |
| 130600 |
Elliptocytosis 2; EL2 |
| 225450 |
Elliptocytosis, Atypical |
| 225500 |
Ellis-Van Creveld Syndrome; EVC (1 mouse model) |
| 609029 |
Emanuel Syndrome |
| 310300 |
Emery-Dreifuss Muscular Dystrophy 1, X-Linked; EDMD1 |
| 181350 |
Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant; EDMD2 (3 mouse models) |
| 612998 |
Emery-Dreifuss Muscular Dystrophy 4, Autosomal Dominant; EDMD4 (1 mouse model) |
| 612999 |
Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant; EDMD5 |
| 614302 |
Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant; EDMD7 |
| 130710 |
Emphysema, Congenital Lobar; CLE |
| 602564 |
Emphysema, Congenital, with Deafness, Penoscrotal Web, and Mental Retardation |
| 130700 |
Emphysema, Hereditary Pulmonary (13 mouse models) |
| 600907 |
Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis |
| 204690 |
Enamel-Renal Syndrome; ERS |
| 613001 |
Encephalocraniocutaneous Lipomatosis; ECCL |
| 225700 |
Encephalomalacia, Multilocular |
| 614520 |
Encephalomyopathy, Mitochondrial, Due to Voltage-Dependent Anion Channel Deficiency |
| 608033 |
Encephalopathy, Acute, Infection-Induced, Susceptibility to, 3; IIAE3 |
| 614212 |
Encephalopathy, Acute, Infection-Induced, Susceptibility to, 4; IIAE4 |
| 225740 |
Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts |
| 602473 |
Encephalopathy, Ethylmalonic; EE (1 mouse model) |
| 604218 |
Encephalopathy, Familial, with Neuroserpin Inclusion Bodies; FENIB (3 mouse models) |
| 614388 |
Encephalopathy, Lethal, Due to Defective Mitochondrial and Peroxisomal Fission; EMPF |
| 300673 |
Encephalopathy, Neonatal Severe, Due to Mecp2 Mutations |
| 130950 |
Encephalopathy, Recurrent, of Childhood |
| 225755 |
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration |
| 166000 |
Enchondromatosis, Multiple, Ollier Type |
| 226100 |
Endocardial Fibroelastosis and Coarctation of Abdominal Aorta |
| 226000 |
Endocardial Fibroelastosis; EFE |
| 612651 |
Endocrine-Cerebroosteodysplasia; ECO |
| 608089 |
Endometrial Cancer (5 mouse models) |
| 131200 |
Endometriosis, Susceptibility to, 1 (1 mouse model) |
| 226110 |
Endothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia |
| 603034 |
Endplate Acetylcholinesterase Deficiency; EAD |
| 268100 |
Enhanced S-Cone Syndrome; ESCS (2 mouse models) |
| 131375 |
Enolase, Sperm Specific; ENO4 |
| 226150 |
Enterocolitis |
| 226200 |
Enterokinase Deficiency |
| 600351 |
Enteropathy, Familial, with Villous Edema and Immunoglobulin G2 Deficiency |
| 226300 |
Enteropathy, Protein-Losing |
| 600631 |
Enuresis, Nocturnal, 1; ENUR1 |
| 600808 |
Enuresis, Nocturnal, 2; ENUR2 |
| 131400 |
Eosinophilia, Familial |
| 226350 |
Eosinophilic Fasciitis |
| 131430 |
Eosinophilopenia |
| 131450 |
Epiblepharon of Lower Lid |
| 131460 |
Epiblepharon of Upper Lid |
| 131500 |
Epicanthus |
| 226400 |
Epidermodysplasia Verruciformis; EV |
| 305350 |
Epidermodysplasia Verruciformis, X-Linked; EDVX; EDV2 |
| 131600 |
Epidermoid Cysts |
| 131750 |
Epidermolysis Bullosa Dystrophica, Autosomal Dominant; DDEB |
| 226600 |
Epidermolysis Bullosa Dystrophica, Autosomal Recessive; RDEB (5 mouse models) |
| 226500 |
Epidermolysis Bullosa Dystrophica Neurotrophica |
| 131850 |
Epidermolysis Bullosa Dystrophica, Pretibial |
| 226700 |
Epidermolysis Bullosa, Junctional, Herlitz Type (3 mouse models) |
| 226730 |
Epidermolysis Bullosa Junctionalis with Pyloric Atresia (1 mouse model) |
| 226650 |
Epidermolysis Bullosa, Junctional, Non-Herlitz Type (5 mouse models) |
| 226440 |
Epidermolysis Bullosa, Late-Onset Localized Junctional, with Mental Retardation |
| 609638 |
Epidermolysis Bullosa, Lethal Acantholytic |
| 615028 |
Epidermolysis Bullosa, Nonspecific, Autosomal Recessive; EBNS |
| 604129 |
Epidermolysis Bullosa Pruriginosa |
| 601001 |
Epidermolysis Bullosa Simplex, Autosomal Recessive (2 mouse models) |
| 131760 |
Epidermolysis Bullosa Simplex, Dowling-Meara Type (4 mouse models) |
| 131900 |
Epidermolysis Bullosa Simplex, Generalized |
| 131800 |
Epidermolysis Bullosa Simplex, Localized |
| 131950 |
Epidermolysis Bullosa Simplex, Ogna Type (4 mouse models) |
| 607600 |
Epidermolysis Bullosa Simplex Superficialis; EBSS |
| 609352 |
Epidermolysis Bullosa Simplex with Migratory Circinate Erythema |
| 131960 |
Epidermolysis Bullosa Simplex with Mottled Pigmentation; EBS-MP |
| 226670 |
Epidermolysis Bullosa Simplex with Muscular Dystrophy (2 mouse models) |
| 612138 |
Epidermolysis Bullosa Simplex with Pyloric Atresia |
| 132000 |
Epidermolysis Bullosa with Congenital Localized Absence of Skin and Deformity of Nails |
| 131880 |
Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase |
| 226735 |
Epidermolysis Bullosa with Diaphragmatic Hernia |
| 113800 |
Epidermolytic Hyperkeratosis; EHK (4 mouse models) |
| 132090 |
Epilepsy, Benign Occipital; BOE |
| 600131 |
Epilepsy, Childhood Absence, Susceptibility to, 1; ECA1 |
| 607681 |
Epilepsy, Childhood Absence, Susceptibility to, 2; ECA2 |
| 612269 |
Epilepsy, Childhood Absence, Susceptibility to, 5; ECA5 |
| 611942 |
Epilepsy, Childhood Absence, Susceptibility to, 6; ECA6 |
| 601068 |
Epilepsy, Familial Adult Myoclonic, 1; FAME1 |
| 607876 |
Epilepsy, Familial Adult Myoclonic, 2; FAME2 |
| 613608 |
Epilepsy, Familial Adult Myoclonic, 3; FAME3 |
| 615127 |
Epilepsy, Familial Adult Myoclonic, 4; FAME4 |
| 600512 |
Epilepsy, Familial Temporal Lobe, 1; ETL1 (4 mouse models) |
| 608096 |
Epilepsy, Familial Temporal Lobe, 2; ETL2 |
| 611630 |
Epilepsy, Familial Temporal Lobe, 3; ETL3 |
| 611631 |
Epilepsy, Familial Temporal Lobe, 4; ETL4 |
| 614417 |
Epilepsy, Familial Temporal Lobe, 5; ETL5 |
| 613339 |
Epilepsy, Hot Water, 1; HWE1 |
| 613340 |
Epilepsy, Hot Water, 2; HWE2 |
| 600669 |
Epilepsy, Idiopathic Generalized; EIG (1 mouse model) |
| 613060 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 10; EIG10 |
| 607628 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 11; EIG11 (1 mouse model) |
| 614847 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 12; EIG12 |
| 606972 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 2; EIG2 |
| 608762 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 3; EIG3 |
| 609750 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 4; EIG4 |
| 611934 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 5; EIG5 |
| 604827 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 7; EIG7 |
| 612899 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 8; EIG8 |
| 607682 |
Epilepsy, Idiopathic Generalized, Susceptibility to, 9; EIG9 |
| 607631 |
Epilepsy, Juvenile Absence, Susceptibility to, 1; EJA1 |
| 611136 |
Epilepsy, Juvenile Myoclonic, Susceptibility to, 5; EJM5 (2 mouse models) |
| 614280 |
Epilepsy, Juvenile Myoclonic, Susceptibility to, 9; EJM9 |
| 254770 |
Epilepsy, Myoclonic Juvenile; EJM (2 mouse models) |
| 600513 |
Epilepsy, Nocturnal Frontal Lobe, 1; ENFL1 |
| 603204 |
Epilepsy, Nocturnal Frontal Lobe, 2; ENFL2 |
| 605375 |
Epilepsy, Nocturnal Frontal Lobe, 3; ENFL3 (1 mouse model) |
| 610353 |
Epilepsy, Nocturnal Frontal Lobe, 4; ENFL4 |
| 615005 |
Epilepsy, Nocturnal Frontal Lobe, 5; ENFL5 |
| 607221 |
Epilepsy, Partial, with Pericentral Spikes; PEPS |
| 604364 |
Epilepsy, Partial, with Variable Foci |
| 226800 |
Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation |
| 612437 |
Epilepsy, Progressive Myoclonic 1B; EPM1B |
| 611726 |
Epilepsy, Progressive Myoclonic 3, with or without Intracellular Inclusions; |
| 254900 |
Epilepsy, Progressive Myoclonic 4, with or without Renal Failure; |
| 613832 |
Epilepsy, Progressive Myoclonic 5; EPM5 |
| 614018 |
Epilepsy, Progressive Myoclonic 6; EPM6 |
| 266100 |
Epilepsy, Pyridoxine-Dependent; EPD |
| 132300 |
Epilepsy, Reading |
| 608105 |
Epilepsy, Rolandic, with Paroxysmal Exercise-Induced Dystonia and Writer's Cramp; EPRPDC |
| 226850 |
Epilepsy-Telangiectasia |
| 226810 |
Epilepsy with Bilateral Occipital Calcifications |
| 613971 |
Epilepsy with Neurodevelopmental Defects; EPND |
| 300491 |
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders |
| 613402 |
Epileptic Encephalopathy, Early Infantile, 10; EIEE10 |
| 613721 |
Epileptic Encephalopathy, Early Infantile, 11; EIEE11 |
| 613722 |
Epileptic Encephalopathy, Early Infantile, 12; EIEE12 |
| 614558 |
Epileptic Encephalopathy, Early Infantile, 13; EIEE13 |
| 614959 |
Epileptic Encephalopathy, Early Infantile, 14; EIEE14 |
| 615006 |
Epileptic Encephalopathy, Early Infantile, 15; EIEE15 |
| 308350 |
Epileptic Encephalopathy, Early Infantile, 1; EIEE1 (3 mouse models) |
| 300672 |
Epileptic Encephalopathy, Early Infantile, 2; EIEE2 |
| 609304 |
Epileptic Encephalopathy, Early Infantile, 3; EIEE3 |
| 612164 |
Epileptic Encephalopathy, Early Infantile, 4; EIEE4 |
| 613477 |
Epileptic Encephalopathy, Early Infantile, 5; EIEE5 |
| 613720 |
Epileptic Encephalopathy, Early Infantile, 7; EIEE7 |
| 300607 |
Epileptic Encephalopathy, Early Infantile, 8; EIEE8 |
| 300088 |
Epileptic Encephalopathy, Early Infantile, 9; EIEE9 |
| 606369 |
Epileptic Encephalopathy, Lennox-Gastaut Type (1 mouse model) |
| 610797 |
Epiphyseal Dysplasia, Baumann Type |
| 226960 |
Epiphyseal Dysplasia, Microcephaly, and Nystagmus |
| 132400 |
Epiphyseal Dysplasia, Multiple, 1; EDM1 (1 mouse model) |
| 600204 |
Epiphyseal Dysplasia, Multiple, 2; EDM2 |
| 600969 |
Epiphyseal Dysplasia, Multiple, 3; EDM3 |
| 226900 |
Epiphyseal Dysplasia, Multiple, 4; EDM4 |
| 607078 |
Epiphyseal Dysplasia, Multiple, 5; EDM5 (1 mouse model) |
| 614135 |
Epiphyseal Dysplasia, Multiple, 6; EDM6 |
| 226980 |
Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus (2 mouse models) |
| 609325 |
Epiphyseal Dysplasia, Multiple, with Miniepiphyses |
| 132450 |
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness; |
| 609324 |
Epiphyseal Dysplasia, Multiple, with Severe Proximal Femoral Dysplasia |
| 226950 |
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness |
| 160120 |
Episodic Ataxia, Type 1; EA1 (1 mouse model) |
| 108500 |
Episodic Ataxia, Type 2; EA2 |
| 606554 |
Episodic Ataxia, Type 3; EA3 |
| 606552 |
Episodic Ataxia, Type 4; EA4 |
| 613855 |
Episodic Ataxia, Type 5; EA5 |
| 612656 |
Episodic Ataxia, Type 6; EA6 |
| 611907 |
Episodic Ataxia, Type 7; EA7 |
| 128200 |
Episodic Kinesigenic Dyskinesia 1; EKD1 |
| 611031 |
Episodic Kinesigenic Dyskinesia 2; EKD2 |
| 300211 |
Episodic Muscle Weakness, X-Linked; EMWX |
| 615040 |
Episodic Pain Syndrome, Familial; FEPS |
| 132500 |
Epistaxis, Hereditary |
| 601315 |
Epithelial Basolateral Chloride Conductance Regulator, Rabbit, Homolog of |
| 122400 |
Epithelial Recurrent Erosion Dystrophy; ERED |
| 226985 |
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract |
| 132810 |
Epoxide Hydrolase 1, Microsomal; EPHX1 |
| 300872 |
Epsilon-Trimethyllysine Hydroxylase Deficiency; TMLHED |
| 132850 |
Epstein-Barr Virus Insertion Site 1; EBVS1 |
| 226990 |
Epstein-Barr Virus, Susceptibility to Chronic Infection By |
| 153650 |
Epstein Syndrome |
| 227010 |
Ermine Phenotype |
| 132990 |
Erythema Nodosum, Familial |
| 227000 |
Erythema of Acral Regions |
| 133000 |
Erythema Palmare Hereditarium |
| 133020 |
Erythermalgia, Primary |
| 612874 |
Erythrocyte Amp Deaminase Deficiency |
| 245340 |
Erythrocyte Lactate Transporter Defect |
| 133100 |
Erythrocytosis, Familial, 1; ECYT1 (2 mouse models) |
| 263400 |
Erythrocytosis, Familial, 2; ECYT2 (1 mouse model) |
| 609820 |
Erythrocytosis, Familial, 3; ECYT3 |
| 611783 |
Erythrocytosis, Familial, 4; ECYT4 |
| 609165 |
Erythroderma, Ichthyosiform, Congenital Reticular; CRIE |
| 227090 |
Erythroderma, Lethal Congenital |
| 133200 |
Erythrokeratodermia Variabilis Et Progressiva; EKVP (1 mouse model) |
| 133180 |
Erythroleukemia, Familial |
| 133239 |
Esophageal Cancer (1 mouse model) |
| 133240 |
Esophageal Ring, Lower |
| 610247 |
Esophagitis, Eosinophilic, 1; EOE1 |
| 613412 |
Esophagitis, Eosinophilic, 2; EOE2 |
| 133260 |
Esterase B; ESB |
| 133270 |
Esterase C; ESC |
| 133300 |
Esterase Es-2, Regulator for |
| 133430 |
Estrogen Receptor 1; ESR1 |
| 227150 |
Ethanolaminosis |
| 600841 |
Eukaryotic Translation Elongation Factor 1 Alpha-1-Like 14; EEF1A1L14 |
| 227200 |
Eunuchoidism, Familial Hypogonadotropic (1 mouse model) |
| 612219 |
Ewing Sarcoma; ES |
| 133500 |
Exchondrosis of Pinna, Posterior |
| 177650 |
Exfoliation Syndrome; XFS (1 mouse model) |
| 607936 |
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-Like |
| 612714 |
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis |
| 133700 |
Exostoses, Multiple, Type I (1 mouse model) |
| 133701 |
Exostoses, Multiple, Type II (1 mouse model) |
| 600209 |
Exostoses, Multiple, Type III; EXT3 |
| 133600 |
Exostoses of Heel |
| 133690 |
Exostoses with Anetodermia and Brachydactyly, Type E |
| 603656 |
Exostosis, Dupuytren Subungual |
| 603439 |
Expansile Bone Lesions |
| 600057 |
Exstrophy of Bladder (1 mouse model) |
| 133705 |
External Auditory Canal, Bilateral Atresia of, with Congenital Vertical Talus |
| 133750 |
Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly |
| 133780 |
Exudative Vitreoretinopathy 1; EVR1 (1 mouse model) |
| 305390 |
Exudative Vitreoretinopathy 2, X-Linked; EVR2 (1 mouse model) |
| 605750 |
Exudative Vitreoretinopathy 3; EVR3 |
| 601813 |
Exudative Vitreoretinopathy 4; EVR4 (1 mouse model) |
| 613310 |
Exudative Vitreoretinopathy 5; EVR5 (1 mouse model) |
| 227210 |
Eyebrows, Duplication of, with Stretchable Skin and Syndactyly |
| 133800 |
Eyebrow, Whorl in |
Analysis Tools