About   Help   FAQ
Due to maintenance, access to MGI may be intermittent starting at 10:00 AM ET Thursday, March 30.
Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

Browse vocabulary terms by beginning character
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9

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: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:242700 T-Cell Immunodeficiency with Thymic Aplasia; TIDTA
OMIM:618398 T-Cell Lymphoma, Subcutaneous Panniculitis-Like; SPTCL
OMIM:618806 T-Cell Lymphopenia, Infantile, with or without Nail Dystrophy, Autosomal Dominant; TLIND
OMIM:186950 T-Cell Subgroups, Non-Hla-Linked
OMIM:187030 T-Complex Locus Tcp10b; TCP10B
OMIM:186890 Tear Protein, Anodal
OMIM:145420 Teebi Hypertelorism Syndrome 1; TBHS1
OMIM:619736 Teebi Hypertelorism Syndrome 2; TBHS2
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, Type 1; HHT1
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:166950 Teratoma, Ovarian
OMIM:273120 Teratoma, Pineal
OMIM:300244 Terminal Osseous Dysplasia; TOD
OMIM:619758 Tessadori-Bicknell-Van Haaften Neurodevelopmental Syndrome 1;
OMIM:619759 Tessadori-Bicknell-Van Haaften Neurodevelopmental Syndrome 2;
OMIM:619950 Tessadori-Bicknell-Van Haaften Neurodevelopmental Syndrome 3;
OMIM:619951 Tessadori-Bicknell-Van Haaften Neurodevelopmental Syndrome 4;
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:187400 Testicular Torsion
OMIM:273395 Tetraamelia Syndrome 1; TETAMS1
OMIM:618021 Tetraamelia Syndrome 2; TETAMS2
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: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:619130 Thrombocytopenia 7; THC7
OMIM:274000 Thrombocytopenia-Absent Radius Syndrome; TAR
OMIM:617441 Thrombocytopenia, Anemia, and Myelofibrosis; THAMY
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:301071 Thrombophilia, X-Linked, Due to Factor VIII Defect; THPH13
OMIM:274150 Thrombotic Thrombocytopenic Purpura, Hereditary; 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: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, 1; THMA1
OMIM:619855 Thyroid Hormone Metabolism, Abnormal, 2; THMA2
OMIM:620198 Thyroid Hormone Metabolism, Abnormal, 3; THMA3
OMIM:188560 Thyroid Hormone Plasma Membrane Transport Defect
OMIM:188570 Thyroid Hormone Resistance, Generalized, Autosomal Dominant; GRTHD
OMIM:274300 Thyroid Hormone Resistance, Generalized, Autosomal Recessive; GRTHR
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: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:618971 Tolchin-Le Caignec Syndrome; TOLCAS
OMIM:275250 Tongue, Pigmented Fungiform Papillae of
OMIM:300978 Tonne-Kalscheuer Syndrome; TOKAS
OMIM:603396 Tonoki Syndrome
OMIM:620173 Tooth Agenesis, Selective, 10; STHAG10
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 1; TBS1
OMIM:617466 Townes-Brocks Syndrome 2; TBS2
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; TALDOD
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; DTGA
OMIM:154500 Treacher Collins Syndrome 1; TCS1
OMIM:613717 Treacher Collins Syndrome 2; TCS2
OMIM:248390 Treacher Collins Syndrome 3; TCS3
OMIM:618939 Treacher Collins Syndrome 4; TCS4
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:618866 Tremor, Hereditary Essential, 6; ETM6
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:618268 Trichohepatoneurodevelopmental Syndrome; THNS
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:618546 Trichothiodystrophy 7, Nonphotosensitive; TTD7
OMIM:619691 Trichothiodystrophy 8, Nonphotosensitive; TTD8
OMIM:619692 Trichothiodystrophy 9, Nonphotosensitive; TTD9
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:618805 Triokinase and Fmn Cyclase Deficiency Syndrome; TKFCD
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:190605 Triphalangeal Thumb with Polysyndactyly; TPTPS
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:162000 Tubulointerstitial Kidney Disease, Autosomal Dominant, 1; ADTKD1
OMIM:174000 Tubulointerstitial Kidney Disease, Autosomal Dominant, 2; ADTKD2
OMIM:613092 Tubulointerstitial Kidney Disease, Autosomal Dominant, 4; ADTKD4
OMIM:617056 Tubulointerstitial Kidney Disease, Autosomal Dominant, 5; ADTKD5
OMIM:607665 Tubulointerstitial Nephritis with Uveitis; TINU
OMIM:191150 Tuftsin Deficiency
OMIM:609428 Tukel Syndrome
OMIM:211900 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1; HFTC1
OMIM:617993 Tumoral Calcinosis, Hyperphosphatemic, Familial, 2; HFTC2
OMIM:617994 Tumoral Calcinosis, Hyperphosphatemic, Familial, 3; HFTC3
OMIM:610455 Tumoral Calcinosis, Normophosphatemic, Familial; NFTC
OMIM:614327 Tumor Predisposition Syndrome 1; TPDS1
OMIM:619975 Tumor Predisposition Syndrome 2; TPDS2
OMIM:603040 Tumor Suppressor Gene on Chromosome 11
OMIM:191200 Tune Deafness
OMIM:618371 Turnpenny-Fry Syndrome; TPFS
OMIM:191250 Twinning Due to Superfetation
OMIM:148500 Tylosis with Esophageal Cancer; TOC
OMIM:601942 Type 1 Diabetes Mellitus 10; T1D10
OMIM:601208 Type 1 Diabetes Mellitus 11; T1D11
OMIM:601388 Type 1 Diabetes Mellitus 12; T1D12
OMIM:601318 Type 1 Diabetes Mellitus 13; T1D13
OMIM:601666 Type 1 Diabetes Mellitus 15; T1D15
OMIM:603266 Type 1 Diabetes Mellitus 17; TID17
OMIM:605598 Type 1 Diabetes Mellitus 18; T1D18
OMIM:610155 Type 1 Diabetes Mellitus 19; T1D19
OMIM:612520 Type 1 Diabetes Mellitus 20; T1D20
OMIM:612521 Type 1 Diabetes Mellitus 21; T1D21
OMIM:612522 Type 1 Diabetes Mellitus 22; T1D22
OMIM:612622 Type 1 Diabetes Mellitus 23; T1D23
OMIM:613006 Type 1 Diabetes Mellitus 24; T1D24
OMIM:125852 Type 1 Diabetes Mellitus 2; T1D2
OMIM:600318 Type 1 Diabetes Mellitus 3; T1D3
OMIM:600319 Type 1 Diabetes Mellitus 4; T1D4
OMIM:600320 Type 1 Diabetes Mellitus 5; T1D5
OMIM:601941 Type 1 Diabetes Mellitus 6; T1D6
OMIM:600321 Type 1 Diabetes Mellitus 7; T1D7
OMIM:600883 Type 1 Diabetes Mellitus 8; T1D8
OMIM:222100 Type 1 Diabetes Mellitus; T1D
OMIM:300136 Type 1 Diabetes Mellitus, X-Linked, Susceptibility To; T1DX
OMIM:616087 Type 2 Diabetes 5; T2D5
OMIM:601283 Type 2 Diabetes Mellitus 1; T2D1
OMIM:601407 Type 2 Diabetes Mellitus 2; T2D2
OMIM:603694 Type 2 Diabetes Mellitus 3; T2D3
OMIM:608036 Type 2 Diabetes Mellitus 4; T2D4
OMIM:125853 Type 2 Diabetes Mellitus; T2D
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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory