| OMIM ID |
Human Disease |
| 207600 |
Takayasu Arteritis |
| 186750 |
Talonavicular Coalition |
| 609655 |
Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals |
| 205400 |
Tangier Disease; TGD (8 mouse models) |
| 272600 |
Tapetoretinal Degeneration with Ataxia |
| 313480 |
Taqi Polymorphism; TAQ1 |
| 272620 |
Tardive Dyskinesia |
| 311900 |
TARP Syndrome; TARPS |
| 186570 |
Tarsal-Carpal Coalition Syndrome; TCC |
| 186850 |
Tarsal Coalition |
| 604867 |
Taste Receptor, Type 2, Member 16; TAS2R16 |
| 272650 |
Tatsumi Factor Deficiency |
| 272700 |
Taurodontism |
| 313490 |
Taurodontism, Microdontia, and Dens Invaginatus |
| 272800 |
Tay-Sachs Disease; TSD (3 mouse models) |
| 607044 |
T-Box 24 |
| 601705 |
T-Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy (3 mouse models) |
| 614868 |
T-Cell Immunodeficiency, Recurrent Infections, and Autoimmunity with or without Cardiac Malformations; TIIAC |
| 186950 |
T-Cell Subgroups, Non-Hla-Linked |
| 187030 |
T-Complex Locus Tcp10b; TCP10B |
| 186890 |
Tear Protein, Anodal |
| 272950 |
Teebi-Shaltout Syndrome |
| 272980 |
Teeth, Congenital Absence of, with Taurodontia and Sparse Hair |
| 273000 |
Teeth, Fused |
| 273050 |
Teeth, Noneruption of, with Maxillary Hypoplasia and Genu Valgum |
| 187000 |
Teeth, Odd Shapes of |
| 187050 |
Teeth Present at Birth |
| 187100 |
Teeth, Supernumerary |
| 187260 |
Telangiectasia, Hereditary Benign |
| 187300 |
Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber; (4 mouse models) |
| 600376 |
Telangiectasia, Hereditary Hemorrhagic, Type 2; HHT2 (4 mouse models) |
| 601101 |
Telangiectasia, Hereditary Hemorrhagic, Type 3; HHT3 |
| 610655 |
Telangiectasia, Hereditary Hemorrhagic, Type 4; HHT4 |
| 187350 |
Telecanthus |
| 187270 |
Telomerase Reverse Transcriptase; TERT |
| 187340 |
Temperature-Sensitive Lethal Mutation |
| 611816 |
Temple-Baraitser Syndrome |
| 187360 |
Temporal Arteritis |
| 605282 |
Temtamy Preaxial Brachydactyly Syndrome; TPBS |
| 187390 |
Tendons, Extensor, of Fingers, Anomalous Insertion of |
| 611426 |
Tented Eyebrows |
| 187395 |
Teratocarcinoma-Derived Growth Factor 1; TDGF1 |
| 166950 |
Teratoma, Ovarian (1 mouse model) |
| 273120 |
Teratoma, Pineal |
| 300244 |
Terminal Osseous Dysplasia; TOD |
| 273150 |
Testes, Rudimentary |
| 300228 |
Testicular Germ Cell Tumor 1; TGCT1 |
| 273300 |
Testicular Germ Cell Tumor; TGCT |
| 610441 |
Testicular Microlithiasis |
| 273250 |
Testicular Regression Syndrome; TRS |
| 187400 |
Testicular Torsion |
| 273395 |
Tetraamelia, Autosomal Recessive |
| 273390 |
Tetraamelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities |
| 187501 |
Tetralogy of Fallot and Glaucoma |
| 605618 |
Tetralogy of Fallot Syndrome, Autosomal Recessive |
| 187500 |
Tetralogy of Fallot; TOF (13 mouse models) |
| 273400 |
Tetramelic Deficiencies, Ectodermal Dysplasia, Deformed Ears, and Other Abnormalities |
| 187510 |
Tetramelic Monodactyly |
| 614846 |
Tetrasomy 15q26 |
| 614290 |
Tetrasomy 18p |
| 608028 |
Thai Symphalangism Syndrome |
| 273490 |
Thalamic Degeneration, Symmetric Infantile |
| 187550 |
Thalassemia, Beta+, Silent Allele |
| 273600 |
Thalidomide Susceptibility |
| 273680 |
Thanatophoric Dysplasia, Glasgow Variant |
| 187601 |
Thanatophoric Dysplasia, Type II; TD2 (2 mouse models) |
| 187600 |
Thanatophoric Dysplasia, Type I; TD1 (3 mouse models) |
| 187650 |
Theophylline Biotransformation |
| 607483 |
Thiamine Metabolism Dysfunction Syndrome 2 (biotin- or Thiamine-Responsive Type); THMD2 |
| 613710 |
Thiamine Metabolism Dysfunction Syndrome 4 (bilateral Striatal Degeneration and Progressive Polyneuropathy Type); THMD4 |
| 614458 |
Thiamine Metabolism Dysfunction Syndrome 5 (episodic Encephalopathy Type); THMD5 |
| 249270 |
Thiamine-Responsive Megaloblastic Anemia Syndrome; TRMA (1 mouse model) |
| 165700 |
Thiemann Disease |
| 610460 |
Thiopurine S-Methyltransferase Deficiency (1 mouse model) |
| 171200 |
Thiourea Tasting |
| 187750 |
Thoracic Dysostosis, Isolated |
| 273730 |
Thoracic Dysplasia-Hydrocephalus Syndrome |
| 313850 |
Thoracoabdominal Syndrome; THAS |
| 187760 |
Thoracolaryngopelvic Dysplasia; TLPD |
| 273740 |
Thoracomelic Dysplasia |
| 187770 |
Thoracopelvic Dysostosis |
| 273750 |
Three M Syndrome 1; 3M1 |
| 612921 |
Three M Syndrome 2; 3M2 |
| 614205 |
Three M Syndrome 3; 3M3 |
| 273770 |
Threoninemia |
| 187900 |
Thrombasthenia-Thrombocytopenia, Hereditary |
| 187940 |
Thrombocyte B; THB |
| 187950 |
Thrombocythemia 1; THCYT1 (1 mouse model) |
| 601977 |
Thrombocythemia 2; THCYT2 |
| 614521 |
Thrombocythemia 3; THCYT3 (2 mouse models) |
| 300331 |
Thrombocythemia, X-Linked; THCYTX |
| 313900 |
Thrombocytopenia 1; THC1 (1 mouse model) |
| 188000 |
Thrombocytopenia 2; THC2 |
| 273900 |
Thrombocytopenia 3; THC3 |
| 612004 |
Thrombocytopenia 4; THC4 |
| 274000 |
Thrombocytopenia-Absent Radius Syndrome; TAR |
| 188020 |
Thrombocytopenia, Cyclic |
| 188025 |
Thrombocytopenia, Paris-Trousseau Type; TCPT |
| 314050 |
Thrombocytopenia with Beta-Thalassemia, X-Linked; XLTT |
| 314000 |
Thrombocytopenia with Elevated Serum Iga and Renal Disease |
| 300367 |
Thrombocytopenia, X-Linked, with or without Dyserythropoietic Anemia; |
| 188030 |
Thrombocytopenic Purpura, Autoimmune; AITP |
| 188055 |
Thrombophilia Due to Activated Protein C Resistance; THPH2 |
| 613116 |
Thrombophilia Due to Histidine-Rich Glycoprotein Deficiency; THPH11 |
| 176860 |
Thrombophilia Due to Protein C Deficiency, Autosomal Dominant; THPH3 |
| 612304 |
Thrombophilia Due to Protein C Deficiency, Autosomal Recessive; THPH4 |
| 612336 |
Thrombophilia Due to Protein S Deficiency, Autosomal Dominant; THPH5 |
| 614514 |
Thrombophilia Due to Protein S Deficiency, Autosomal Recessive; THPH6 |
| 188050 |
Thrombophilia Due to Thrombin Defect; THPH1 |
| 614486 |
Thrombophilia Due to Thrombomodulin Defect; THPH12 (1 mouse model) |
| 612348 |
Thrombophilia, Familial, Due to Decreased Release of Tissue Plasminogen Activator; THPH9 |
| 300807 |
Thrombophilia, X-Linked, Due to Factor IX Defect; THPH8 |
| 274150 |
Thrombotic Thrombocytopenic Purpura, Congenital; TTP (1 mouse model) |
| 274190 |
Thumb Agenesis, Short Stature, and Immunodeficiency |
| 188100 |
Thumb Deformity |
| 188150 |
Thumb Deformity and Alopecia |
| 274200 |
Thumb, Distal Hyperextensibility of |
| 274205 |
Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness |
| 314100 |
Thumbs, Congenital Clasped |
| 188201 |
Thumbs, Stiff, with Brachydactyly Type A1 and Developmental Delay |
| 274210 |
Thymic Aplasia with Fetal Death |
| 274265 |
Thymic-Renal-Anal-Lung Dysplasia |
| 274230 |
Thymoma, Familial |
| 274240 |
Thyrocerebroretinal Syndrome |
| 188455 |
Thyroglossal Duct Cyst, Familial |
| 155240 |
Thyroid Carcinoma, Familial Medullary; MTC (1 mouse model) |
| 188470 |
Thyroid Carcinoma, Follicular; FTC (4 mouse models) |
| 607464 |
Thyroid Carcinoma, Hurthle Cell |
| 606240 |
Thyroid Carcinoma, Nonmedullary, Susceptibility to, 1 |
| 603386 |
Thyroid Carcinoma, Nonmedullary, with or without Cell Oxyphilia |
| 188550 |
Thyroid Carcinoma, Papillary |
| 605642 |
Thyroid Carcinoma, Papillary, with Papillary Renal Neoplasia |
| 274400 |
Thyroid Dyshormonogenesis 1; TDH1 |
| 274500 |
Thyroid Dyshormonogenesis 2A; TDH2A |
| 274700 |
Thyroid Dyshormonogenesis 3; TDH3 (1 mouse model) |
| 274800 |
Thyroid Dyshormonogenesis 4; TDH4 |
| 274900 |
Thyroid Dyshormonogenesis 5; TDH5 |
| 607200 |
Thyroid Dyshormonogenesis 6; TDH6 (1 mouse model) |
| 609698 |
Thyroid Hormone Metabolism, Abnormal |
| 188560 |
Thyroid Hormone Plasma Membrane Transport Defect |
| 188570 |
Thyroid Hormone Resistance, Generalized, Autosomal Dominant; GRTH (5 mouse models) |
| 274300 |
Thyroid Hormone Resistance, Generalized, Autosomal Recessive; GRTH (2 mouse models) |
| 145650 |
Thyroid Hormone Resistance, Selective Pituitary; PRTH |
| 612306 |
Thyroid-Stimulating Hormone Level Quantitative Trait Locus 1; TSHQTL1 |
| 603372 |
Thyroid-Stimulating Hormone Receptor; TSHR |
| 188580 |
Thyrotoxic Periodic Paralysis, Susceptibility to, 1; TTPP1 |
| 613239 |
Thyrotoxic Periodic Paralysis, Susceptibility to, 2; TTPP2 |
| 614834 |
Thyrotoxic Periodic Paralysis, Susceptibility to, 3; TTPP3 |
| 275120 |
Thyrotropin-Releasing Hormone Deficiency |
| 188545 |
Thyrotropin-Releasing Hormone Receptor; TRHR (1 mouse model) |
| 314200 |
Thyroxine-Binding Globulin of Serum; TBG |
| 275230 |
Tibia, Absence of, with Congenital Deafness |
| 188740 |
Tibia, Absence of, with Polydactyly |
| 601027 |
Tibia, Absence or Hypoplasia of, with Polydactyly, Retrocerebellar Arachnoid Cyst, and Other Anomalies |
| 609143 |
Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum |
| 188770 |
Tibia, Hypoplasia of, with Polydactyly |
| 275220 |
Tibial Hemimelia |
| 600334 |
Tibial Muscular Dystrophy, Tardive (1 mouse model) |
| 188800 |
Tibial Torsion, Bilateral Medial |
| 103500 |
Tietz Syndrome (14 mouse models) |
| 275190 |
Tiglic Acidemia |
| 601005 |
Timothy Syndrome; TS (1 mouse model) |
| 275240 |
Tinea Imbricata, Susceptibility to |
| 188850 |
Tl Antigen |
| 300622 |
Tn Polyagglutination Syndrome; TNPS |
| 188890 |
Tobacco Addiction, Susceptibility to |
| 189000 |
Toe, Fifth, Number of Phalanges in |
| 189100 |
Toe, Misshapen |
| 189150 |
Toe, Rotated Fifth |
| 189200 |
Toes, Relative Length of First and Second |
| 189230 |
Toes, Space Between First and Second |
| 300707 |
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations; |
| 603030 |
Toll-Like Receptor 4; TLR4 (5 mouse models) |
| 189300 |
Tongue Curling, Folding, or Rolling |
| 275250 |
Tongue, Pigmented Fungiform Papillae of |
| 603396 |
Tonoki Syndrome |
| 106600 |
Tooth Agenesis, Selective, 1; STHAG1 (3 mouse models) |
| 602639 |
Tooth Agenesis, Selective, 2; STHAG2 |
| 604625 |
Tooth Agenesis, Selective, 3; STHAG3 (2 mouse models) |
| 150400 |
Tooth Agenesis, Selective, 4; STHAG4 |
| 610926 |
Tooth Agenesis, Selective, 5; STHAG5 |
| 613097 |
Tooth Agenesis, Selective, 6; STHAG6 |
| 313500 |
Tooth Agenesis, Selective, X-Linked, 1; STHAGX1 |
| 314240 |
Tooth Size |
| 259600 |
Torg-Winchester Syndrome |
| 613600 |
Torsade De Pointes, Short-Coupled Variant |
| 602554 |
Torsion Dystonia with Onset in Infancy |
| 189600 |
Torticollis |
| 314300 |
Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia; TKCR |
| 189700 |
Torus Palatinus and Torus Mandibularis |
| 106700 |
Total Anomalous Pulmonary Venous Return 1; TAPVR1 |
| 107480 |
Townes-Brocks Syndrome; TBS (3 mouse models) |
| 603569 |
Tracheobronchial Stenosis, Congenital |
| 275300 |
Tracheobronchomegaly |
| 189960 |
Tracheoesophageal Fistula with or without Esophageal Atresia (1 mouse model) |
| 189961 |
Tracheopathia Osteoplastica |
| 606003 |
Transaldolase Deficiency |
| 193090 |
Transcobalamin I Deficiency |
| 275350 |
Transcobalamin II Deficiency |
| 614193 |
Transferrin Serum Level Quantitative Trait Locus 2; TFQTL2 |
| 131705 |
Transient Bullous Dermolysis of the Newborn; TBDN |
| 227050 |
Transient Erythroblastopenia of Childhood; TEC |
| 608808 |
Transposition of the Great Arteries, Dextro-Looped 1; DTGA1 (4 mouse models) |
| 613853 |
Transposition of the Great Arteries, Dextro-Looped 2; DTGA2 |
| 613854 |
Transposition of the Great Arteries, Dextro-Looped 3; DTGA3 |
| 600952 |
Transsexuality |
| 154500 |
Treacher Collins Syndrome 1; TCS1 (2 mouse models) |
| 613717 |
Treacher Collins Syndrome 2; TCS2 |
| 248390 |
Treacher Collins Syndrome 3; TCS3 |
| 612119 |
Trehalase Deficiency |
| 190300 |
Tremor, Hereditary Essential, 1; ETM1 |
| 602134 |
Tremor, Hereditary Essential, 2; ETM2 |
| 611456 |
Tremor, Hereditary Essential, 3; ETM3 |
| 614782 |
Tremor, Hereditary Essential, 4; ETM4 |
| 611808 |
Tremor, Hereditary Essential, and Idiopathic Normal Pressure Hydrocephalus; |
| 190310 |
Tremor, Nystagmus, and Duodenal Ulcer |
| 190200 |
Tremor of Intention, Ataxia, and Lipofuscinosis |
| 275370 |
Tricarboxylic Acid Cycle, Defect of |
| 609649 |
Trichilemmal Cyst 1; TRICY1 |
| 601453 |
Trichodental Dysplasia |
| 190320 |
Trichodentoosseous Syndrome |
| 190360 |
Trichodysplasia-Xeroderma |
| 601606 |
Trichoepithelioma, Multiple Familial, 1 |
| 612099 |
Trichoepithelioma, Multiple Familial, 2 |
| 190345 |
Trichoepitheliomas, Multiple Desmoplastic |
| 222470 |
Trichohepatoenteric Syndrome 1; THES1 |
| 614602 |
Trichohepatoenteric Syndrome 2; THES2 |
| 190330 |
Trichomegaly |
| 275400 |
Trichomegaly with Mental Retardation, Dwarfism, and Pigmentary Degeneration of Retina |
| 275450 |
Trichoodontoonychial Dysplasia with Bone Deficiency |
| 190351 |
Trichorhinophalangeal Syndrome, Type III; TRPS3 |
| 150230 |
Trichorhinophalangeal Syndrome, Type II; TRPS2 |
| 190350 |
Trichorhinophalangeal Syndrome, Type I; TRPS1 (1 mouse model) |
| 275550 |
Trichorrhexis Nodosa Syndrome |
| 609990 |
Trichoscyphodysplasia |
| 234050 |
Trichothiodystrophy, Nonphotosensitive 1; TTDN1 |
| 601675 |
Trichothiodystrophy, Photosensitive; TTDP (3 mouse models) |
| 613229 |
Trichotillomania; TTM (1 mouse model) |
| 605067 |
Tricuspid Atresia (1 mouse model) |
| 609015 |
Trifunctional Protein Deficiency (1 mouse model) |
| 190400 |
Trigeminal Neuralgia |
| 190410 |
Trigger Thumb |
| 190420 |
Triglyceride Storage Disease, Type I |
| 190430 |
Triglyceride Storage Disease, Type II |
| 275595 |
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet |
| 190440 |
Trigonocephaly 1; TRIGNO1 |
| 614485 |
Trigonocephaly 2; TRIGNO2 |
| 314320 |
Trigonocephaly with Short Stature and Developmental Delay |
| 602079 |
Trimethylaminuria; TMAU |
| 190450 |
Triosephosphate Isomerase 1; TPI1 |
| 190600 |
Triphalangeal Thumb, Nonopposable |
| 190650 |
Triphalangeal Thumbs and Dislocation of Patella |
| 190680 |
Triphalangeal Thumbs with Brachyectrodactyly |
| 190500 |
Triphalangeal Thumb with Double Phalanges |
| 601161 |
Trisomy 18-Like Syndrome |
| 190800 |
Tristichiasis |
| 190900 |
Tritanopia |
| 191000 |
Trochlea of the Humerus, Aplasia of |
| 608189 |
Tropical Calcific Pancreatitis |
| 614044 |
Trypsinogen Deficiency |
| 276100 |
Tryptophanuria with Dwarfism |
| 276200 |
T-Substance Anomaly |
| 613636 |
Tuberculin Skin Test Reactivity, Absence of |
| 613637 |
Tuberculin Skin Test Reactivity Quantitative Trait Locus |
| 191100 |
Tuberous Sclerosis 1; TSC1 (8 mouse models) |
| 613254 |
Tuberous Sclerosis 2; TSC2 (7 mouse models) |
| 301850 |
Tubulin, Beta |
| 607665 |
Tubulointerstitial Nephritis with Uveitis; TINU |
| 191150 |
Tuftsin Deficiency |
| 609428 |
Tukel Syndrome |
| 211900 |
Tumoral Calcinosis, Hyperphosphatemic, Familial; HFTC (2 mouse models) |
| 610455 |
Tumoral Calcinosis, Normophosphatemic, Familial; NFTC |
| 614327 |
Tumor Predisposition Syndrome; TPDS |
| 603040 |
Tumor Suppressor Gene on Chromosome 11 |
| 191200 |
Tune Deafness |
| 191250 |
Twinning Due to Superfetation |
| 276410 |
Twinning, Monozygotic |
| 148500 |
Tylosis with Esophageal Cancer; TOC |
| 611521 |
Tyrosine Kinase 2 Deficiency |
| 276700 |
Tyrosinemia, Type I (3 mouse models) |
| 276600 |
Tyrosinemia, Type II |
| 276710 |
Tyrosinemia, Type III (1 mouse model) |
| 276800 |
Tyrosinosis |
| 615102 |
Tyshchenko Syndrome |
Analysis Tools