| OMIM ID |
Human Disease |
| 301500 |
Fabry Disease (1 mouse model) |
| 227250 |
Facial Abnormalities, Kyphoscoliosis, and Mental Retardation |
| 600251 |
Facial Clefting, Oblique, 1; OBLFC1 |
| 602556 |
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly |
| 615139 |
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature; FILS |
| 603589 |
Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification |
| 227255 |
Facial Dysmorphism with Multiple Malformations |
| 134000 |
Facial Hypertrichosis |
| 134200 |
Facial Palsy, Familial Recurrent Peripheral |
| 601471 |
Facial Paresis, Hereditary Congenital, 1; HCFP1 |
| 604185 |
Facial Paresis, Hereditary Congenital, 2; HCFP2 |
| 614744 |
Facial Paresis, Hereditary Congenital, 3; HCFP3 |
| 134300 |
Facial Spasm |
| 227270 |
Faciocardiomelic Dysplasia, Lethal |
| 612731 |
Faciocardiomelic Syndrome |
| 227280 |
Faciocardiorenal Syndrome |
| 227330 |
Faciodigitogenital Syndrome, Recessive |
| 158900 |
Facioscapulohumeral Muscular Dystrophy 1; FSHD1 (3 mouse models) |
| 158901 |
Facioscapulohumeral Muscular Dystrophy 2; FSHD2 |
| 227320 |
Faciothoracogenital Syndrome |
| 134540 |
Factor IX and Factor XI, Combined Deficiency of |
| 134520 |
Factors VIII, IX and XI, Combined Deficiency of |
| 227300 |
Factor V and Factor VIII, Combined Deficiency of, 1; F5F8D1 |
| 613625 |
Factor V and Factor VIII, Combined Deficiency of, 2; F5F8D2 |
| 227310 |
Factor V and Factor VIII, Combined Deficiency of, with Normal Protein C and Protein C Inhibitor |
| 227400 |
Factor V Deficiency |
| 134400 |
Factor V Excess with Spontaneous Thrombosis |
| 134430 |
Factor VII and Factor VIII, Combined Deficiency of |
| 227500 |
Factor VII Deficiency |
| 134510 |
Factor VIII and Factor IX, Combined Deficiency Of; F8F9D |
| 134500 |
Factor VIII Deficiency |
| 227600 |
Factor X Deficiency (3 mouse models) |
| 612416 |
Factor XI Deficiency |
| 234000 |
Factor XII Deficiency |
| 613225 |
Factor XIII, A Subunit, Deficiency of (2 mouse models) |
| 613235 |
Factor XIII, B Subunit, Deficiency of |
| 125350 |
Failure of Tooth Eruption, Primary; PFE |
| 601127 |
Fallot Complex with Severe Mental and Growth Retardation |
| 175100 |
Familial Adenomatous Polyposis 1; FAP1 (5 mouse models) |
| 608456 |
Familial Adenomatous Polyposis, 2; FAP2 |
| 120100 |
Familial Cold Autoinflammatory Syndrome 1; FCAS1 (2 mouse models) |
| 611762 |
Familial Cold Autoinflammatory Syndrome 2; FCAS2 |
| 614468 |
Familial Cold Autoinflammatory Syndrome 3; FCAS3 |
| 174810 |
Familial Expansile Osteolysis; FEO |
| 134610 |
Familial Mediterranean Fever, Autosomal Dominant |
| 249100 |
Familial Mediterranean Fever; FMF (5 mouse models) |
| 227650 |
Fanconi Anemia, Complementation Group A; FANCA (3 mouse models) |
| 300514 |
Fanconi Anemia, Complementation Group B; FANCB |
| 227645 |
Fanconi Anemia, Complementation Group C; FANCC (2 mouse models) |
| 605724 |
Fanconi Anemia, Complementation Group D1; FANCD1 (1 mouse model) |
| 227646 |
Fanconi Anemia, Complementation Group D2; FANCD2 (5 mouse models) |
| 600901 |
Fanconi Anemia, Complementation Group E; FANCE |
| 603467 |
Fanconi Anemia, Complementation Group F; FANCF |
| 614082 |
Fanconi Anemia, Complementation Group G; FANCG |
| 609053 |
Fanconi Anemia, Complementation Group I; FANCI |
| 609054 |
Fanconi Anemia, Complementation Group J; FANCJ |
| 614083 |
Fanconi Anemia, Complementation Group L; FANCL |
| 614087 |
Fanconi Anemia, Complementation Group M; FANCM |
| 610832 |
Fanconi Anemia, Complementation Group N; FANCN |
| 613390 |
Fanconi Anemia, Complementation Group O; FANCO |
| 613951 |
Fanconi Anemia, Complementation Group P; FANCP |
| 227810 |
Fanconi-Bickel Syndrome; FBS |
| 227850 |
Fanconi-Like Syndrome |
| 134600 |
Fanconi Renotubular Syndrome 1; FRTS1 |
| 613388 |
Fanconi Renotubular Syndrome 2; FRTS2 |
| 228000 |
Farber Lipogranulomatosis (1 mouse model) |
| 228020 |
Fascial Dystrophy, Congenital |
| 606035 |
Fasting Insulin Level Quantitative Trait Locus 1; FIQTL1 |
| 613462 |
Fasting Plasma Glucose Level Quantitative Trait Locus 4; FGQTL4 |
| 613463 |
Fasting Plasma Glucose Level Quantitative Trait Locus 5; FGQTL5 |
| 613460 |
Fasting Plasma Glucose Level Quantitative Trait Locus 6; FGQTL6 |
| 600072 |
Fatal Familial Insomnia; FFI (1 mouse model) |
| 602935 |
Fatty Acid Amide Hydrolase; FAAH |
| 613282 |
Fatty Liver Disease, Nonalcoholic, Susceptibility to, 1; NAFLD1 (3 mouse models) |
| 613387 |
Fatty Liver Disease, Nonalcoholic, Susceptibility to, 2; NAFLD2 |
| 134700 |
Favism, Susceptibility to |
| 211500 |
Fazio-Londe Disease |
| 612637 |
Febrile Seizures, Familial, 10 |
| 614418 |
Febrile Seizures, Familial, 11; FEB11 |
| 121210 |
Febrile Seizures, Familial, 1; FEB1 |
| 602477 |
Febrile Seizures, Familial, 2; FEB2 |
| 604352 |
Febrile Seizures, Familial, 4; FEB4 |
| 609255 |
Febrile Seizures, Familial, 5; FEB5 |
| 609253 |
Febrile Seizures, Familial, 6; FEB6 |
| 611515 |
Febrile Seizures, Familial, 7; FEB7 |
| 611634 |
Febrile Seizures, Familial, 9; FEB9 |
| 153640 |
Fechtner Syndrome; FTNS |
| 164280 |
Feingold Syndrome 1; FGLDS1 |
| 614326 |
Feingold Syndrome 2; FGLDS2 (1 mouse model) |
| 134750 |
Felty Syndrome |
| 134780 |
Femoral-Facial Syndrome; FFS |
| 228200 |
Femur-Fibula-Ulna Syndrome |
| 228250 |
Femur, Unilateral Bifid, with Monodactylous Ectrodactyly |
| 134770 |
Ferritin Heavy Chain 1; FTH1 |
| 228300 |
Fertile Eunuch Syndrome |
| 208150 |
Fetal Akinesia Deformation Sequence; FADS |
| 300073 |
Fetal Akinesia Syndrome, X-Linked |
| 228355 |
Fetal Iodine Deficiency Disorder; FIDD |
| 228400 |
Fever, Familial Lifelong Persistent |
| 300321 |
FG Syndrome 2; FGS2 |
| 300406 |
FG Syndrome 3; FGS3 |
| 300422 |
Fg Syndrome 4; FGS4 |
| 300581 |
Fg Syndrome 5; FGS5 |
| 134820 |
Fibrinogen, A Alpha Polypeptide; FGA |
| 134900 |
Fibrinolytic Defect |
| 228520 |
Fibrochondrogenesis 1; FBCG1 |
| 614524 |
Fibrochondrogenesis 2; FBCG2 |
| 135100 |
Fibrodysplasia Ossificans Progressiva; FOP (1 mouse model) |
| 228550 |
Fibromatosis, Congenital Generalized; CGF |
| 135300 |
Fibromatosis, Gingival, 1; GINGF1 |
| 605544 |
Fibromatosis, Gingival, 2; GINGF2 |
| 609955 |
Fibromatosis, Gingival, 3; GINGF3 |
| 611010 |
Fibromatosis, Gingival, 4; GINGF4 |
| 228560 |
Fibromatosis, Gingival, with Distinctive Facies |
| 605400 |
Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation |
| 135550 |
Fibromatosis, Gingival, with Progressive Deafness |
| 135580 |
Fibromuscular Dysplasia of Arteries |
| 228800 |
Fibrosclerosis, Multifocal |
| 135700 |
Fibrosis of Extraocular Muscles, Congenital, 1; CFEOM1 |
| 602078 |
Fibrosis of Extraocular Muscles, Congenital, 2; CFEOM2 |
| 600638 |
Fibrosis of Extraocular Muscles, Congenital, 3a, with or without Extraocular Involvement; CFEOM3A (1 mouse model) |
| 609384 |
Fibrosis of Extraocular Muscles, Congenital, 3c; CFEOM3C |
| 609612 |
Fibrosis of Extraocular Muscles, Congenital, with Synergistic Divergence |
| 228930 |
Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly (2 mouse models) |
| 246570 |
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome |
| 135800 |
Fibula, Recurrent Dislocation of Head of |
| 228900 |
Fibular Hypoplasia and Complex Brachydactyly |
| 228940 |
Fibuloulnar Aplasia or Hypoplasia with Renal Abnormalities |
| 135950 |
Finger Locking, Recurrent, with Intrauterine Growth Retardation and Proportionate Short Stature |
| 305550 |
Fingerprint Body Myopathy |
| 136100 |
Fingers, Relative Length of |
| 136120 |
Fish-Eye Disease; FED (1 mouse model) |
| 270710 |
Fitzsimmons-Guilbert Syndrome |
| 228980 |
Fleck Retina, Familial Benign; FRFB |
| 228990 |
Fleck Retina of Kandori |
| 136140 |
Floating-Harbor Syndrome; FLHS |
| 136150 |
Flood Factor Deficiency |
| 136200 |
Flushing of Ears and Somnolence |
| 136300 |
Flynn-Aird Syndrome |
| 607341 |
Focal Cortical Dysplasia of Taylor; FCDT |
| 305600 |
Focal Dermal Hypoplasia; FDH (8 mouse models) |
| 136400 |
Focal Epithelial Hyperplasia of the Oral Mucosa |
| 229045 |
Focal Epithelial Hyperplasia, Oral |
| 136500 |
Focal Facial Dermal Dysplasia 1, Brauer Type; FFDD1 |
| 614973 |
Focal Facial Dermal Dysplasia 2, Brauer-Setleis Type; FFDD2 |
| 227260 |
Focal Facial Dermal Dysplasia 3, Setleis Type; FFDD3 (1 mouse model) |
| 614974 |
Focal Facial Dermal Dysplasia 4; FFDD4 |
| 603278 |
Focal Segmental Glomerulosclerosis 1; FSGS1 (1 mouse model) |
| 603965 |
Focal Segmental Glomerulosclerosis 2; FSGS2 (3 mouse models) |
| 607832 |
Focal Segmental Glomerulosclerosis 3, Susceptibility To; FSGS3 (1 mouse model) |
| 612551 |
Focal Segmental Glomerulosclerosis 4, Susceptibility To; FSGS4 |
| 613237 |
Focal Segmental Glomerulosclerosis 5; FSGS5 |
| 614131 |
Focal Segmental Glomerulosclerosis 6; FSGS6 |
| 601775 |
Folate Level in Erythrocytes |
| 229050 |
Folate Malabsorption, Hereditary |
| 229070 |
Follicle-Stimulating Hormone Deficiency, Isolated |
| 603587 |
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts |
| 613024 |
Follicular Lymphoma, Susceptibility to, 1; FL1 |
| 229100 |
Formiminotransferase Deficiency |
| 613606 |
Forsythe-Wakeling Syndrome; FWS |
| 229120 |
Fountain Syndrome |
| 136480 |
Fourth Cranial Nerve Palsy, Familial Congenital |
| 609218 |
Foveal Hypoplasia and Anterior Segment Dysgenesis; FHASD |
| 136520 |
Foveal Hypoplasia and Presenile Cataract Syndrome |
| 136540 |
Fragile Site 10q23 |
| 136560 |
Fragile Site 11q13 |
| 136580 |
Fragile Site 16q22; FRA16A |
| 300624 |
Fragile X Mental Retardation Syndrome (8 mouse models) |
| 300623 |
Fragile X Tremor/Ataxia Syndrome; FXTAS (2 mouse models) |
| 249420 |
Frank-Ter Haar Syndrome; FTHS (1 mouse model) |
| 229230 |
Fraser-Like Syndrome |
| 219000 |
Fraser Syndrome (14 mouse models) |
| 136680 |
Frasier Syndrome |
| 229250 |
Freesia Flowers, Inability to Smell |
| 609640 |
Frias Syndrome |
| 229300 |
Friedreich Ataxia 1; FRDA (3 mouse models) |
| 601992 |
Friedreich Ataxia 2; FRDA2 |
| 229310 |
Friedreich Ataxia and Congenital Glaucoma |
| 136600 |
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness |
| 229400 |
Frontofacionasal Dysplasia |
| 305620 |
Frontometaphyseal Dysplasia; FMD |
| 136760 |
Frontonasal Dysplasia 1; FND1 |
| 613451 |
Frontonasal Dysplasia 2; FND2 |
| 613456 |
Frontonasal Dysplasia 3; FND3 |
| 203000 |
Frontonasal Dysplasia with Alar Clefts |
| 605321 |
Frontoocular Syndrome |
| 105550 |
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis; FTDALS |
| 600795 |
Frontotemporal Dementia, Chromosome 3-Linked; FTD3 |
| 600274 |
Frontotemporal Dementia; FTD (10 mouse models) |
| 607485 |
Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related (3 mouse models) |
| 229700 |
Fructose-1,6-Bisphosphatase Deficiency |
| 229500 |
Fructose and Galactose Intolerance |
| 229600 |
Fructose Intolerance, Hereditary |
| 229650 |
Fructose Utilization |
| 229800 |
Fructosuria, Essential |
| 606155 |
Fryns-Aftimos Syndrome |
| 600302 |
Fryns Macrocephaly |
| 600776 |
Fryns Microphthalmia Syndrome |
| 229850 |
Fryns Syndrome; FRNS |
| 136830 |
Fucosidase Regulator |
| 230000 |
Fucosidosis |
| 182100 |
Fucosyltransferase 2; FUT2 |
| 613852 |
Fucosyltransferase 6 Deficiency |
| 606812 |
Fumarase Deficiency |
| 136880 |
Fundus Albipunctatus (1 mouse model) |
| 136900 |
Fundus Dystrophy, Pseudoinflammatory, of Sorsby; SFD (2 mouse models) |
| 264420 |
Fundus Dystrophy, Pseudoinflammatory, Recessive Form |
| 137000 |
Futcher Line |
Analysis Tools