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

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Human Diseases/Syndromes Beginning with "T"

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OMIM ID	Human 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:620641	Tan-Almurshedi Syndrome; TANALS
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; TMDI
OMIM:272800	Tay-Sachs Disease; TSD
OMIM:607044	T-Box 24
OMIM:601705	T-Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy;
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:610655	Telangiectasia, Hereditary Hemorrhagic, Type 4; HHT4
OMIM:615506	Telangiectasia, Hereditary Hemorrhagic, Type 5; HHT5
OMIM:621056	Telangiectasia, Impaired Intellectual Development, Microcephaly, Metaphyseal Dysplasia, Eye Abnormalities, and Short Stature; TIMES
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: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:620484	Thrombocytopenia 10; THC10
OMIM:620654	Thrombocytopenia 11 with Multiple Congenital Anomalies and Dysmorphic Facies; THC11
OMIM:620757	Thrombocytopenia 12 with or without Myopathy; THC12
OMIM:620776	Thrombocytopenia 13, Syndromic; THC13
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:620475	Thrombocytopenia 8, with Dysmorphic Features and Developmental Delay;
OMIM:620478	Thrombocytopenia 9; THC9
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: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: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:601552	Traboulsi Syndrome
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; TCN1D
OMIM:275350	Transcobalamin II Deficiency; TCN2D
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; MFT1
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:613627	Tsukahara Syndrome
OMIM:603438	Tsukahara Syndrome
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:621106	Tubulointerstitial Kidney Disease, Autosomal Dominant 6; ADTKD6
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:615848	Tumor Predisposition Syndrome 3; TPDS3
OMIM:609265	Tumor Predisposition Syndrome 4; TPDS4
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

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