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Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

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Human Diseases/Syndromes Beginning with "T"

To see all annotations for a disease, click the disease name.

OMIM IDHuman 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
615879 Tatton-Brown-Rahman Syndrome; TBRS
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
615387 T-Cell Receptor-Alpha/Beta Deficiency
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
615506 Telangiectasia, Hereditary Hemorrhagic, Type 5; HHT5
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
218340 Temtamy Syndrome; TEMTYS
187390 Tendons, Extensor, of Fingers, Anomalous Insertion of
611426 Tented Eyebrows
187395 Teratocarcinoma-Derived Growth Factor 1; TDGF1
166950 Teratoma, Ovarian (2 mouse models)
273120 Teratoma, Pineal
300244 Terminal Osseous Dysplasia; TOD
273150 Testes, Rudimentary
615542 Testicular Anomalies with or without Congenital Heart Disease; TACHD
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 models)
165700 Thiemann Disease
610460 Thiopurine S-Methyltransferase Deficiency (1 mouse models)
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
187940 Thrombocyte B; THB
187950 Thrombocythemia 1; THCYT1 (1 mouse models)
601977 Thrombocythemia 2; THCYT2
614521 Thrombocythemia 3; THCYT3 (3 mouse models)
300331 Thrombocythemia, X-Linked; THCYTX
313900 Thrombocytopenia 1; THC1 (1 mouse models)
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 models)
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 models)
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 models)
188470 Thyroid Carcinoma, Follicular; FTC (5 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 (2 mouse models)
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 models)
274800 Thyroid Dyshormonogenesis 4; TDH4
274900 Thyroid Dyshormonogenesis 5; TDH5
607200 Thyroid Dyshormonogenesis 6; TDH6 (1 mouse models)
609698 Thyroid Hormone Metabolism, Abnormal
188560 Thyroid Hormone Plasma Membrane Transport Defect
188570 Thyroid Hormone Resistance, Generalized, Autosomal Dominant; GRTH (7 mouse models)
274300 Thyroid Hormone Resistance, Generalized, Autosomal Recessive; GRTH (2 mouse models)
145650 Thyroid Hormone Resistance, Selective Pituitary; PRTH
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 models)
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 models)
188800 Tibial Torsion, Bilateral Medial
103500 Tietz Syndrome (14 mouse models)
275190 Tiglic Acidemia
601005 Timothy Syndrome; TS (1 mouse models)
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)
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
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 models)
189961 Tracheopathia Osteoplastica
606003 Transaldolase Deficiency
193090 Transcobalamin I Deficiency
275350 Transcobalamin II Deficiency
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; TDO
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; TCMGLY
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 models)
275550 Trichorrhexis Nodosa Syndrome
609990 Trichoscyphodysplasia
234050 Trichothiodystrophy, Nonphotosensitive 1; TTDN1
601675 Trichothiodystrophy, Photosensitive; TTDP (3 mouse models)
613229 Trichotillomania; TTM (1 mouse models)
605067 Tricuspid Atresia (1 mouse models)
609015 Trifunctional Protein Deficiency (1 mouse models)
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
615512 Triosephosphate Isomerase Deficiency; TPID
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
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
148500 Tylosis with Esophageal Cancer; TOC
611521 Tyrosine Kinase 2 Deficiency
276710 Tyrosinemia, Type III; TYRSN3 (1 mouse models)
276600 Tyrosinemia, Type II; TYRSN2
276700 Tyrosinemia, Type I; TYRSN1 (4 mouse models)
276800 Tyrosinosis
615102 Tyshchenko Syndrome

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last database update
08/12/2014
MGI 5.19
The Jackson Laboratory