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: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
|