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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
OMIM:207600 Takayasu Arteritis
OMIM:616737 Takenouchi-Kosaki Syndrome; TKS
OMIM:186750 Talonavicular Coalition
OMIM:609655 Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals
OMIM:205400 Tangier Disease; TGD
OMIM:272600 Tapetoretinal Degeneration with Ataxia
OMIM:313480 Taqi Polymorphism; TAQ1
OMIM:272620 Tardive Dyskinesia
OMIM:311900 TARP Syndrome; TARPS
OMIM:186570 Tarsal-Carpal Coalition Syndrome; TCC
OMIM:186850 Tarsal Coalition
OMIM:604867 Taste Receptor, Type 2, Member 16; TAS2R16
OMIM:272650 Tatsumi Factor Deficiency
OMIM:615879 Tatton-Brown-Rahman Syndrome; TBRS
OMIM:272700 Taurodontism
OMIM:313490 Taurodontism, Microdontia, and Dens Invaginatus
OMIM:272800 Tay-Sachs Disease; TSD
OMIM:607044 T-Box 24
OMIM:601705 T-Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
OMIM:614868 T-Cell Immunodeficiency, Recurrent Infections, and Autoimmunity with or without Cardiac Malformations; TIIAC
OMIM:615387 T-Cell Receptor-Alpha/Beta Deficiency
OMIM:186950 T-Cell Subgroups, Non-Hla-Linked
OMIM:187030 T-Complex Locus Tcp10b; TCP10B
OMIM:186890 Tear Protein, Anodal
OMIM:272950 Teebi-Shaltout Syndrome; TBSH
OMIM:272980 Teeth, Congenital Absence of, with Taurodontia and Sparse Hair
OMIM:273000 Teeth, Fused
OMIM:273050 Teeth, Noneruption of, with Maxillary Hypoplasia and Genu Valgum
OMIM:187000 Teeth, Odd Shapes of
OMIM:187050 Teeth Present at Birth
OMIM:187100 Teeth, Supernumerary
OMIM:187260 Telangiectasia, Hereditary Benign
OMIM:187300 Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber;
OMIM:600376 Telangiectasia, Hereditary Hemorrhagic, Type 2; HHT2
OMIM:601101 Telangiectasia, Hereditary Hemorrhagic, Type 3; HHT3
OMIM:610655 Telangiectasia, Hereditary Hemorrhagic, Type 4; HHT4
OMIM:615506 Telangiectasia, Hereditary Hemorrhagic, Type 5; HHT5
OMIM:187350 Telecanthus
OMIM:187340 Temperature-Sensitive Lethal Mutation
OMIM:611816 Temple-Baraitser Syndrome; TMBTS
OMIM:616222 Temple Syndrome
OMIM:187360 Temporal Arteritis
OMIM:605282 Temtamy Preaxial Brachydactyly Syndrome; TPBS
OMIM:218340 Temtamy Syndrome; TEMTYS
OMIM:187390 Tendons, Extensor, of Fingers, Anomalous Insertion of
OMIM:616260 Tenorio Syndrome; TNORS
OMIM:611426 Tented Eyebrows
OMIM:187395 Teratocarcinoma-Derived Growth Factor 1; TDGF1
OMIM:166950 Teratoma, Ovarian
OMIM:273120 Teratoma, Pineal
OMIM:300244 Terminal Osseous Dysplasia; TOD
OMIM:273150 Testes, Rudimentary
OMIM:615542 Testicular Anomalies with or without Congenital Heart Disease; TACHD
OMIM:300228 Testicular Germ Cell Tumor 1; TGCT1
OMIM:273300 Testicular Germ Cell Tumor; TGCT
OMIM:610441 Testicular Microlithiasis
OMIM:273250 Testicular Regression Syndrome; TRS
OMIM:187400 Testicular Torsion
OMIM:273395 Tetraamelia Syndrome, Autosomal Recessive; TETAMS
OMIM:273390 Tetraamelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities
OMIM:187501 Tetralogy of Fallot and Glaucoma
OMIM:605618 Tetralogy of Fallot Syndrome, Autosomal Recessive
OMIM:187500 Tetralogy of Fallot; TOF
OMIM:273400 Tetramelic Deficiencies, Ectodermal Dysplasia, Deformed Ears, and Other Abnormalities
OMIM:187510 Tetramelic Monodactyly
OMIM:614846 Tetrasomy 15q26
OMIM:614290 Tetrasomy 18p
OMIM:608028 Thai Symphalangism Syndrome
OMIM:273490 Thalamic Degeneration, Symmetric Infantile
OMIM:187550 Thalassemia, Beta+, Silent Allele
OMIM:273600 Thalidomide Susceptibility
OMIM:273680 Thanatophoric Dysplasia, Glasgow Variant
OMIM:187601 Thanatophoric Dysplasia, Type II; TD2
OMIM:187600 Thanatophoric Dysplasia, Type I; TD1
OMIM:617107 Thauvin-Robinet-Faivre Syndrome; TROFAS
OMIM:187650 Theophylline Biotransformation
OMIM:607483 Thiamine Metabolism Dysfunction Syndrome 2 (biotin- or Thiamine-Responsive Type); THMD2
OMIM:613710 Thiamine Metabolism Dysfunction Syndrome 4 (bilateral Striatal Degeneration and Progressive Polyneuropathy Type); THMD4
OMIM:614458 Thiamine Metabolism Dysfunction Syndrome 5 (episodic Encephalopathy Type); THMD5
OMIM:249270 Thiamine-Responsive Megaloblastic Anemia Syndrome; TRMA
OMIM:165700 Thiemann Disease
OMIM:610460 Thiopurines, Poor Metabolism of, 1; THPM1
OMIM:616903 Thiopurines, Poor Metabolism of, 2; THPM2
OMIM:187750 Thoracic Dysostosis, Isolated
OMIM:273730 Thoracic Dysplasia-Hydrocephalus Syndrome
OMIM:313850 Thoracoabdominal Syndrome; THAS
OMIM:187760 Thoracolaryngopelvic Dysplasia; TLPD
OMIM:273740 Thoracomelic Dysplasia
OMIM:187770 Thoracopelvic Dysostosis
OMIM:273750 Three M Syndrome 1; 3M1
OMIM:612921 Three M Syndrome 2; 3M2
OMIM:614205 Three M Syndrome 3; 3M3
OMIM:273770 Threoninemia
OMIM:187950 Thrombocythemia 1; THCYT1
OMIM:601977 Thrombocythemia 2; THCYT2
OMIM:614521 Thrombocythemia 3; THCYT3
OMIM:300331 Thrombocythemia, X-Linked; THCYTX
OMIM:313900 Thrombocytopenia 1; THC1
OMIM:188000 Thrombocytopenia 2; THC2
OMIM:273900 Thrombocytopenia 3; THC3
OMIM:612004 Thrombocytopenia 4; THC4
OMIM:616216 Thrombocytopenia 5; THC5
OMIM:616937 Thrombocytopenia 6; THC6
OMIM:274000 Thrombocytopenia-Absent Radius Syndrome; TAR
OMIM:188020 Thrombocytopenia, Cyclic
OMIM:188025 Thrombocytopenia, Paris-Trousseau Type; TCPT
OMIM:314050 Thrombocytopenia with Beta-Thalassemia, X-Linked; XLTT
OMIM:314000 Thrombocytopenia with Elevated Serum Iga and Renal Disease
OMIM:300367 Thrombocytopenia, X-Linked, with or without Dyserythropoietic Anemia;
OMIM:188030 Thrombocytopenic Purpura, Autoimmune; AITP
OMIM:188055 Thrombophilia Due to Activated Protein C Resistance; THPH2
OMIM:613116 Thrombophilia Due to Histidine-Rich Glycoprotein Deficiency; THPH11
OMIM:176860 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant; THPH3
OMIM:612304 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive; THPH4
OMIM:612336 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant; THPH5
OMIM:614514 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive; THPH6
OMIM:188050 Thrombophilia Due to Thrombin Defect; THPH1
OMIM:614486 Thrombophilia Due to Thrombomodulin Defect; THPH12
OMIM:612348 Thrombophilia, Familial, Due to Decreased Release of Tissue Plasminogen Activator; THPH9
OMIM:300807 Thrombophilia, X-Linked, Due to Factor IX Defect; THPH8
OMIM:274150 Thrombotic Thrombocytopenic Purpura, Congenital; TTP
OMIM:274190 Thumb Agenesis, Short Stature, and Immunodeficiency
OMIM:188100 Thumb Deformity
OMIM:188150 Thumb Deformity and Alopecia
OMIM:274200 Thumb, Distal Hyperextensibility of
OMIM:274205 Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness
OMIM:314100 Thumbs, Congenital Clasped
OMIM:188201 Thumbs, Stiff, with Brachydactyly Type A1 and Developmental Delay
OMIM:274210 Thymic Aplasia with Fetal Death
OMIM:274265 Thymic-Renal-Anal-Lung Dysplasia
OMIM:274230 Thymoma, Familial
OMIM:274240 Thyrocerebroretinal Syndrome
OMIM:188455 Thyroglossal Duct Cyst, Familial
OMIM:188550 Thyroid Cancer, Nonmedullary, 1; NMTC1
OMIM:188470 Thyroid Cancer, Nonmedullary, 2; NMTC2
OMIM:606240 Thyroid Cancer, Nonmedullary, 3; NMTC3
OMIM:616534 Thyroid Cancer, Nonmedullary, 4; NMTC4
OMIM:616535 Thyroid Cancer, Nonmedullary, 5; NMTC5
OMIM:155240 Thyroid Carcinoma, Familial Medullary; MTC
OMIM:607464 Thyroid Carcinoma, Hurthle Cell
OMIM:603386 Thyroid Carcinoma, Nonmedullary, with or without Cell Oxyphilia
OMIM:605642 Thyroid Carcinoma, Papillary, with Papillary Renal Neoplasia
OMIM:274400 Thyroid Dyshormonogenesis 1; TDH1
OMIM:274500 Thyroid Dyshormonogenesis 2A; TDH2A
OMIM:274700 Thyroid Dyshormonogenesis 3; TDH3
OMIM:274800 Thyroid Dyshormonogenesis 4; TDH4
OMIM:274900 Thyroid Dyshormonogenesis 5; TDH5
OMIM:607200 Thyroid Dyshormonogenesis 6; TDH6
OMIM:609698 Thyroid Hormone Metabolism, Abnormal
OMIM:188560 Thyroid Hormone Plasma Membrane Transport Defect
OMIM:188570 Thyroid Hormone Resistance, Generalized, Autosomal Dominant; GRTH
OMIM:274300 Thyroid Hormone Resistance, Generalized, Autosomal Recessive; GRTH
OMIM:145650 Thyroid Hormone Resistance, Selective Pituitary; PRTH
OMIM:603372 Thyroid-Stimulating Hormone Receptor; TSHR
OMIM:188580 Thyrotoxic Periodic Paralysis, Susceptibility to, 1; TTPP1
OMIM:613239 Thyrotoxic Periodic Paralysis, Susceptibility to, 2; TTPP2
OMIM:614834 Thyrotoxic Periodic Paralysis, Susceptibility to, 3; TTPP3
OMIM:275120 Thyrotropin-Releasing Hormone Deficiency
OMIM:188545 Thyrotropin-Releasing Hormone Receptor; TRHR
OMIM:275230 Tibia, Absence of, with Congenital Deafness
OMIM:601027 Tibia, Absence or Hypoplasia of, with Polydactyly, Retrocerebellar Arachnoid Cyst, and Other Anomalies
OMIM:188740 Tibia, Hypoplasia or Aplasia of, with Polydactyly; THYP
OMIM:275220 Tibial Hemimelia
OMIM:600334 Tibial Muscular Dystrophy, Tardive; TMD
OMIM:188800 Tibial Torsion, Bilateral Medial
OMIM:103500 Tietz Albinism-Deafness Syndrome; TADS
OMIM:275190 Tiglic Acidemia
OMIM:601005 Timothy Syndrome; TS
OMIM:275240 Tinea Imbricata, Susceptibility to
OMIM:188850 Tl Antigen
OMIM:300622 Tn Polyagglutination Syndrome; TNPS
OMIM:188890 Tobacco Addiction, Susceptibility to
OMIM:189000 Toe, Fifth, Number of Phalanges in
OMIM:189100 Toe, Misshapen
OMIM:189150 Toe, Rotated Fifth
OMIM:189200 Toes, Relative Length of First and Second
OMIM:189230 Toes, Space Between First and Second
OMIM:300707 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations;
OMIM:275250 Tongue, Pigmented Fungiform Papillae of
OMIM:603396 Tonoki Syndrome
OMIM:106600 Tooth Agenesis, Selective, 1; STHAG1
OMIM:602639 Tooth Agenesis, Selective, 2; STHAG2
OMIM:604625 Tooth Agenesis, Selective, 3; STHAG3
OMIM:150400 Tooth Agenesis, Selective, 4; STHAG4
OMIM:610926 Tooth Agenesis, Selective, 5; STHAG5
OMIM:616724 Tooth Agenesis, Selective, 7; STHAG7
OMIM:617073 Tooth Agenesis, Selective, 8; STHAG8
OMIM:617275 Tooth Agenesis, Selective, 9; STHAG9
OMIM:313500 Tooth Agenesis, Selective, X-Linked, 1; STHAGX1
OMIM:613600 Torsade De Pointes, Short-Coupled Variant
OMIM:602554 Torsion Dystonia with Onset in Infancy
OMIM:189600 Torticollis
OMIM:314300 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia; TKCR
OMIM:189700 Torus Palatinus and Torus Mandibularis
OMIM:106700 Total Anomalous Pulmonary Venous Return 1; TAPVR1
OMIM:107480 Townes-Brocks Syndrome; TBS
OMIM:603569 Tracheobronchial Stenosis, Congenital
OMIM:275300 Tracheobronchomegaly
OMIM:189960 Tracheoesophageal Fistula with or without Esophageal Atresia
OMIM:189961 Tracheopathia Osteoplastica
OMIM:606003 Transaldolase Deficiency
OMIM:193090 Transcobalamin I Deficiency
OMIM:275350 Transcobalamin II Deficiency
OMIM:131705 Transient Bullous Dermolysis of the Newborn; TBDN
OMIM:227050 Transient Erythroblastopenia of Childhood; TEC
OMIM:608808 Transposition of the Great Arteries, Dextro-Looped 1; DTGA1
OMIM:613854 Transposition of the Great Arteries, Dextro-Looped 3; DTGA3
OMIM:154500 Treacher Collins Syndrome 1; TCS1
OMIM:613717 Treacher Collins Syndrome 2; TCS2
OMIM:248390 Treacher Collins Syndrome 3; TCS3
OMIM:612119 Trehalase Deficiency
OMIM:190300 Tremor, Hereditary Essential, 1; ETM1
OMIM:602134 Tremor, Hereditary Essential, 2; ETM2
OMIM:611456 Tremor, Hereditary Essential, 3; ETM3
OMIM:614782 Tremor, Hereditary Essential, 4; ETM4
OMIM:616736 Tremor, Hereditary Essential, 5; ETM5
OMIM:611808 Tremor, Hereditary Essential, and Idiopathic Normal Pressure Hydrocephalus;
OMIM:190310 Tremor, Nystagmus, and Duodenal Ulcer
OMIM:190200 Tremor of Intention, Ataxia, and Lipofuscinosis
OMIM:275370 Tricarboxylic Acid Cycle, Defect of
OMIM:609649 Trichilemmal Cyst 1; TRICY1
OMIM:601453 Trichodental Dysplasia
OMIM:190320 Trichodentoosseous Syndrome; TDO
OMIM:190360 Trichodysplasia-Xeroderma
OMIM:601606 Trichoepithelioma, Multiple Familial, 1
OMIM:612099 Trichoepithelioma, Multiple Familial, 2
OMIM:190345 Trichoepitheliomas, Multiple Desmoplastic
OMIM:222470 Trichohepatoenteric Syndrome 1; THES1
OMIM:614602 Trichohepatoenteric Syndrome 2; THES2
OMIM:190330 Trichomegaly; TCMGLY
OMIM:275450 Trichoodontoonychial Dysplasia with Bone Deficiency
OMIM:190351 Trichorhinophalangeal Syndrome, Type III; TRPS3
OMIM:150230 Trichorhinophalangeal Syndrome, Type II; TRPS2
OMIM:190350 Trichorhinophalangeal Syndrome, Type I; TRPS1
OMIM:609990 Trichoscyphodysplasia
OMIM:601675 Trichothiodystrophy 1, Photosensitive; TTD1
OMIM:616390 Trichothiodystrophy 2, Photosensitive; TTD2
OMIM:616395 Trichothiodystrophy 3, Photosensitive; TTD3
OMIM:234050 Trichothiodystrophy 4, Nonphotosensitive; TTD4
OMIM:300953 Trichothiodystrophy 5, Nonphotosensitive; TTD5
OMIM:616943 Trichothiodystrophy 6, Nonphotosensitive; TTD6
OMIM:613229 Trichotillomania; TTM
OMIM:605067 Tricuspid Atresia
OMIM:190400 Trigeminal Neuralgia
OMIM:190410 Trigger Thumb
OMIM:190420 Triglyceride Storage Disease, Type I
OMIM:190430 Triglyceride Storage Disease, Type II
OMIM:275595 Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet
OMIM:190440 Trigonocephaly 1; TRIGNO1
OMIM:614485 Trigonocephaly 2; TRIGNO2
OMIM:314320 Trigonocephaly with Short Stature and Developmental Delay
OMIM:602079 Trimethylaminuria; TMAU
OMIM:615512 Triosephosphate Isomerase Deficiency; TPID
OMIM:190600 Triphalangeal Thumb, Nonopposable
OMIM:190650 Triphalangeal Thumbs and Dislocation of Patella
OMIM:190680 Triphalangeal Thumbs with Brachyectrodactyly
OMIM:190500 Triphalangeal Thumb with Double Phalanges
OMIM:601161 Trisomy 18-Like Syndrome
OMIM:190800 Tristichiasis
OMIM:190900 Tritanopia
OMIM:191000 Trochlea of the Humerus, Aplasia of
OMIM:608189 Tropical Calcific Pancreatitis
OMIM:614044 Trypsinogen Deficiency
OMIM:276100 Tryptophanuria with Dwarfism
OMIM:276200 T-Substance Anomaly
OMIM:613636 Tuberculin Skin Test Reactivity, Absence of
OMIM:191100 Tuberous Sclerosis 1; TSC1
OMIM:613254 Tuberous Sclerosis 2; TSC2
OMIM:301850 Tubulin, Beta
OMIM:607665 Tubulointerstitial Nephritis with Uveitis; TINU
OMIM:191150 Tuftsin Deficiency
OMIM:609428 Tukel Syndrome
OMIM:211900 Tumoral Calcinosis, Hyperphosphatemic, Familial; HFTC
OMIM:610455 Tumoral Calcinosis, Normophosphatemic, Familial; NFTC
OMIM:614327 Tumor Predisposition Syndrome; TPDS
OMIM:603040 Tumor Suppressor Gene on Chromosome 11
OMIM:191200 Tune Deafness
OMIM:191250 Twinning Due to Superfetation
OMIM:148500 Tylosis with Esophageal Cancer; TOC
OMIM:276710 Tyrosinemia, Type III; TYRSN3
OMIM:276600 Tyrosinemia, Type II; TYRSN2
OMIM:276700 Tyrosinemia, Type I; TYRSN1
OMIM:276800 Tyrosinosis
OMIM:615102 Tyshchenko Syndrome

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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory