Disease Name Symbol Acronym
T Cell Deficiency TCL003
T-B+ Severe Combined Immunodeficiency Due to Cd3delta/cd3epsilon/cd3zeta TBS005
T-Cell Acute Lymphocytic Leukemia-1 TCL017
T-Cell Adult Acute Lymphocytic Leukemia TCL001
T-Cell Immunodeficiency with Epidermodysplasia Verruciformis TCL011
T-Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy TCL016
T-Cell Immunodeficiency, Recurrent Infections, Autoimmunity, and Cardiac Malformations TCL014
T-Cell Large Granular Lymphocyte Leukemia TCL002
T-Cell Leukemia TCL004
T-Cell Prolymphocytic Leukemia TCL005
T-Cell/histiocyte Rich Large B Cell Lymphoma TCL012
Tabes Dorsalis TBS001
Tac3-Related Isolated Gonadotropin-Releasing Hormone Deficiency TC3001
Tacr3-Related Isolated Gonadotropin-Releasing Hormone Deficiency TCR001
Tacrolimus Dose Selection TCR004
Tactile Agnosia TCT002
Taeniasis TNS007
Takayasu Arteritis TKY002
Takenouchi-Kosaki Syndrome TKN001
Talipes Equinovarus TLP001
Tall Cell Variant Papillary Carcinoma TLL001
Tangier Disease TNG002
Tanycytic Ependymoma TNY001
Tardbp-Related Amyotrophic Lateral Sclerosis TRD001
Tardbp-Related Frontotemporal Dementia TRD005
Tardive Dyskinesia TRD006
Tarp Syndrome TRP006
Tarsal Tunnel Syndrome TRS001
Tarsal-Carpal Coalition Syndrome TRS002
Tatton-Brown-Rahman Syndrome TTT001
Tauopathy TPT001
Taurodontism TRD003
Tay-Sachs Disease TYS001
Tay-Sachs Disease, B Variant, Adult Form TYS006
Tay-Sachs Disease, B Variant, Infantile Form TYS004
Tay-Sachs Disease, B Variant, Juvenile Form TYS003
Tay-Sachs Disease, B1 Variant TYS005
Taylor's Syndrome TYL001
Taz-Related Dilated Cardiomyopathy TZR001
Tbc1d24-Related Disorders TBC002
Tbx5-Related Holt-Oram Syndrome TBX001
Tcap-Related Dilated Cardiomyopathy TCP001
Tcap-Related Familial Hypertrophic Cardiomyopathy TCP002
Tcf12-Related Craniosynostosis TCF002
Tcirg1-Related Autosomal Recessive Osteopetrosis TCR002
Tcof1-Related Treacher Collins Syndrome TCF001
Tctn1-Related Joubert Syndrome TCT003
Tctn2-Related Joubert Syndrome TCT004
Tctn2-Related Meckel Syndrome TCT005
Teeth Hard Tissue Disease TTH005
Telangiectasia Macularis Eruptiva Perstans TLN012
Telangiectasia, Hereditary Hemorrhagic, Type 1 TLN006
Telangiectasia, Hereditary Hemorrhagic, Type 2 TLN011
Telangiectasia, Hereditary Hemorrhagic, Type 3 TLN009
Telangiectasia, Hereditary Hemorrhagic, Type 4 TLN010
Telangiectasia, Hereditary Hemorrhagic, Type 5 TLN008
Telangiectasis TLN003
Telangiectatic Osteogenic Sarcoma TLN002
Telogen Effluvium TLG001
Temple Syndrome TMP012
Temple-Baraitser Syndrome TMP011
Temporal Arteritis TMP003
Temporal Lobe Epilepsy TMP001
Temtamy Preaxial Brachydactyly Syndrome TMT002
Temtamy Syndrome TMT003
Tendinitis TND005
Tendinopathy TND004
Tendinosis TND006
Tenorio Syndrome TNR001
Tenosynovial Giant Cell Tumor TNS001
Tenosynovitis TNS014
Teratocarcinoma TRT001
Teratoma TRT010
Terc-Related Dyskeratosis Congenita TRC065
Terc-Related Familial Pulmonary Fibrosis TRC066
Terminal Osseous Dysplasia TRM011
Tert-Related Dyskeratosis Congenita TRT008
Tert-Related Familial Pulmonary Fibrosis TRT009
Tertiary Neurosyphilis TRT002
Tertiary Syphilis TRT003
Testicular Anomalies with or Without Congenital Heart Disease TST035
Testicular Cancer TST014
Testicular Disease TST015
Testicular Fibroma TST012
Testicular Germ Cell Cancer TST026
Testicular Germ Cell Tumor TST021
Testicular Gonadoblastoma TST005
Testicular Granulosa Cell Tumor TST016
Testicular Infarct TST007
Testicular Leukemia TST003
Testicular Leydig Cell Tumor TST001
Testicular Lymphoma TST004
Testicular Malignant Germ Cell Cancer TST017
Testicular Microlithiasis TST025
Testicular Regression Syndrome TST033
Testicular Seminoma TST043
Testicular Spermatocytic Seminoma TST010
Testicular Thecoma TST013
Testicular Trophoblastic Tumor TST040
Testicular Yolk Sac Tumor TST018
Testis Seminoma TST020
Testotoxicosis TST023
Tetanus TTN003
Tetanus Neonatorum TTN001
Tethered Spinal Cord Syndrome TTH004
Tetra-Amelia Syndrome TTR016
Tetrahydrobiopterin Deficiency TTR005
Tetrahydrobiopterin-Responsive Hyperphenylalaninemia/phenylketonuria TTR020
Tetralogy of Fallot TTR001
Tetraploidy TTR011
Tetrasomy 18p TTR014
Tetrasomy 21 TTR021
Tfr2-Related Hereditary Hemochromatosis TFR001
Tgbfr2-Related Lynch Syndrome TGB001
Tgfb2-Related Loeys-Dietz Syndrome TGF006
Tgfb3-Related Loeys-Dietz Syndrome TGF008
Tgfbr1-Related Loeys-Dietz Syndrome TGF001
Tgfbr1-Related Thoracic Aortic Aneurysms and Aortic Dissections TGF002
Tgfbr2-Related Loeys-Dietz Syndrome TGF003
Tgfbr2-Related Thoracic Aortic Aneurysms and Aortic Dissections TGF004
Tgif1-Related Holoprosencephaly TGF005
Tgm1-Related Autosomal Recessive Congenital Ichthyosis TGM001
Thalassemia THL005
Thalassemia Intermedia THL017
Thalassemia Major THL018
Thalassemia Minor THL010
Thalassemia-Beta, Dominant Inclusion-Body THL011
Thalassemia, Hispanic Gamma-Delta-Beta THL013
Thalassemias, Alpha- THL016
Thanatophoric Dysplasia, Type I THN009
Thanatophoric Dysplasia, Type Ii THN010
Thbd-Related Atypical Hemolytic-Uremic Syndrome THB001
Theileriasis THL004
Thiamine Metabolism Dysfunction Syndrome 2 THM010
Thiamine Metabolism Dysfunction Syndrome 4 THM014
Thiamine Metabolism Dysfunction Syndrome 5 THM013
Thiamine-Responsive Megaloblastic Anemia Syndrome THM002
Third Cranial Nerve Disease THR010
Third-Degree Atrioventricular Block THR099
Thomsen and Becker Disease THM017
Thoracic Aortic Aneurysm THR003
Thoracic Aortic Aneurysms and Aortic Dissections THR027
Thoracic Benign Neoplasm THR011
Thoracic Outlet Syndrome THR013
Thoracoabdominal Syndrome THR017
Thoracolumbosacral Spina Bifida Aperta THR085
Thoracolumbosacral Spina Bifida Cystica THR084
Thpo-Related Essential Thrombocythemia THP002
Thrombasthenia THR035
Thrombasthenia of Glanzmann and Naegeli, Itga2b-Related THR046
Thrombasthenia of Glanzmann and Naegeli, Itgb3-Related THR047
Thrombocythemia 1 THR090
Thrombocythemia 2 THR087
Thrombocythemia 3 THR086
Thrombocythemia, X-Linked THR098
Thrombocytopenia THR014
Thrombocytopenia 2 THR037
Thrombocytopenia 4 THR048
Thrombocytopenia 5 THR102
Thrombocytopenia Due to Platelet Alloimmunization THR001
Thrombocytopenia with Beta-Thalassemia, X-Linked THR051
Thrombocytopenia with or Without Dyserythropoietic Anemia THR108
Thrombocytopenia-Absent Radius Syndrome THR009
Thrombocytopenia, Congenital Amegakaryocytic THR103
Thrombocytopenia, Neonatal Alloimmune THR095
Thrombocytopenia, Paris-Trousseau Type THR101
Thrombocytopenia, X-Linked THR042
Thrombocytopenia, X-Linked, with or Without Dyserythropoietic Anemia THR097
Thrombocytopenic Purpura, Autoimmune THR100
Thrombocytosis THR004
Thrombophilia THR015
Thrombophilia Due to Activated Protein C Resistance THR082
Thrombophilia Due to Antithrombin Iii Deficiency THR104
Thrombophilia Due to Heparin Cofactor Ii Deficiency THR020
Thrombophilia Due to Hrg Deficiency THR021
Thrombophilia Due to Protein C Deficiency, Autosomal Dominant THR067
Thrombophilia Due to Protein C Deficiency, Autosomal Recessive THR068
Thrombophilia Due to Protein S Deficiency, Autosomal Dominant THR089
Thrombophilia Due to Protein S Deficiency, Autosomal Recessive THR088
Thrombophilia Due to Thrombin Defect THR092
Thrombophilia Due to Thrombomodulin Defect THR023
Thrombophilia, Familial, Due to Decreased Release of Plat THR060
Thrombophilia, X-Linked, Due to Factor Ix Defect THR055
Thrombophlebitis THR016
Thrombotic Thrombocytopenic Purpura THR005
Thrombotic Thrombocytopenic Purpura, Acquired THR044
Thrombotic Thrombocytopenic Purpura, Familial THR054
Thromboxane Synthase Deficiency THR025
Thryoid Dyshormonogenesis 6 THR063
Thymic Dysplasia THY003
Thymic Epithelial Tumor THY042
Thymic Hyperplasia THY043
Thymoma THY023
Thymus Adenocarcinoma THY024
Thymus Cancer THY025
Thymus Gland Disease THY026
Thymus Large Cell Carcinoma THY005
Thymus Lipoma THY007
Thymus Lymphoma THY006
Thymus Mucoepidermoid Carcinoma THY010
Thyroid Angiosarcoma THY004
Thyroid Cancer THY028
Thyroid Cancer, Anaplastic THY049
Thyroid Cancer, Monmedullary, 1 THY103
Thyroid Cancer, Nonmedullary, 2 THY102
Thyroid Cancer, Nonmedullary, 4 THY100
Thyroid Cancer, Nonmedullary, 5 THY101
Thyroid Carcinoma Somatic THY104
Thyroid Carcinoma with Thyrotoxicosis THY036
Thyroid Carcinoma, Hurthle Cell THY096
Thyroid Carcinoma, Papillary, with Papillary Renal Neoplasia THY065
Thyroid Crisis THY001
Thyroid Dyshormonogenesis 1 THY071
Thyroid Dyshormonogenesis 2a THY061
Thyroid Dyshormonogenesis 3 THY056
Thyroid Dyshormonogenesis 4 THY063
Thyroid Dyshormonogenesis 5 THY062
Thyroid Ectopia THY098
Thyroid Gland Disease THY030
Thyroid Hormone Metabolism, Abnormal THY064
Thyroid Hormone Resistance THY097
Thyroid Hormone Resistance, Autosomal Recessive THY068
Thyroid Hormone Resistance, Selective Pituitary THY069
Thyroid Hormonogenesis Defect I THY057
Thyroid Hurthle Cell Adenoma THY016
Thyroid Lymphoma THY009
Thyroid Sarcoma THY031
Thyroiditis THY032
Thyrotoxic Periodic Paralysis THY054
Thyrotoxic Periodic Paralysis 1 THY084
Thyrotoxic Periodic Paralysis 2 THY083
Thyrotropin-Releasing Hormone Deficiency THY039
Thyroxine-Binding Globulin Deficiency THY041
Tibial Adamantinoma TBL006
Tibial Hemimelia TBL008
Tibial Hemimelia, Bilateral TBL017
Tibial Muscular Dystrophy, Tardive TBL022
Tibial Nerve Palsy TBL001
Tibial Neuropathy TBL007
Tic Disorder TCD001
Tick Infestation TCK004
Tick Paralysis TCK002
Tick-Borne Encephalitis TCK001
Tick-Borne Relapsing Fever TCK003
Tietz Albinism-Deafness Syndrome TTZ003
Timothy Grass Allergy TMT006
Timothy Syndrome TMT001
Timothy Syndrome Type 1 TMT004
Tinea Barbae TNB001
Tinea Capitis TNC002
Tinea Corporis TNC003
Tinea Cruris TNC001
Tinea Favosa TNF001
Tinea Manuum TNM002
Tinea Nigra TNN001
Tinea Pedis TNP001
Tinea Profunda TNP002
Tinea Unguium TNN002
Tinf2-Related Dyskeratosis Congenita TNF003
Tjp2-Related Familial Hypercholanemia TJP001
Tk2-Related Mitochondrial Dna Depletion Syndrome, Myopathic Form TK2001
Tmem127-Related Susceptibility to Pheochromocytoma TMM001
Tmem138-Related Joubert Syndrome TMM002
Tmem216-Related Joubert Syndrome TMM003
Tmem216-Related Meckel Syndrome TMM004
Tmem231-Related Meckel Syndrome TMM014
Tmem237-Related Joubert Syndrome TMM005
Tmem38b-Related Osteogenesis Imperfecta TMM010
Tmem43-Related Emery-Dreifuss Muscular Dystrophy, Autosomal TMM011
Tmem67-Related Joubert Syndrome TMM006
Tmem67-Related Meckel Syndrome TMM007
Tmpo-Related Dilated Cardiomyopathy TMP007
Tn Polyagglutination Syndrome, Somatic TNP003
Tnfrsf11a- Related Autosomal Recessive Osteopetrosis TNF004
Tnfrsf13b-Related Common Variable Immune Deficiency TNF006
Tnfrsf13c-Related Common Variable Immune Deficiency TNF007
Tnfsf11-Related Autosomal Recessive Osteopetrosis TNF005
Tnnc1-Related Dilated Cardiomyopathy TNN003
Tnnc1-Related Familial Hypertrophic Cardiomyopathy TNN004
Tnni2-Related Arthrogryposis Multiplex Congenita, Distal, Type 2b TNN005
Tnni3-Related Dilated Cardiomyopathy TNN006
Tnni3-Related Familial Hypertrophic Cardiomyopathy TNN007
Tnni3-Related Familial Restrictive Cardiomyopathy TNN008
Tnnt1-Related Nemaline Myopathy TNN009
Tnnt2-Related Dilated Cardiomyopathy TNN010
Tnnt2-Related Familial Hypertrophic Cardiomyopathy TNN011
Tnnt2-Related Familial Restrictive Cardiomyopathy TNN012
Tnnt3-Related Arthrogryposis Multiplex Congenita, Distal, Type 2b TNN013
Toenail Dystrophy, Isolated TNL002
Tolosa-Hunt Syndrome TLS001
Tomato Allergy TMT007
Tongue Cancer TNG003
Tongue Disease TNG004
Tongue Squamous Cell Carcinoma TNG009
Tonsil Cancer TNS004
Tonsil Squamous Cell Carcinoma TNS013
Tonsillitis TNS005
Tooth Agenesis TTH002
Tooth Agenesis Selective 7 TTH024
Tooth Agenesis, Selective, 1, with or Without Orofacial Cleft TTH016
Tooth Agenesis, Selective, 2 TTH011
Tooth Agenesis, Selective, 3 TTH012
Tooth Agenesis, Selective, 4 TTH013
Tooth Agenesis, Selective, 5 TTH017
Tooth Agenesis, Selective, X-Linked 1 TTH018
Tooth Ankylosis TTH001
Tooth Disease TTH006
Tooth Erosion TTH007
Tooth Resorption TTH008
Topographical Agnosia TPG001
Topors-Related Retinitis Pigmentosa TPR001
Torch Syndrome TRC034
Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia TRT015
Total Anomalous Pulmonary Venous Return TTL010
Total Spina Bifida Aperta TTL009
Total Spina Bifida Cystica TTL008
Townes-Brocks Syndrome TWN003
Toxic Diffuse Goiter TXC004
Toxic Encephalopathy TXC002
Toxic Maculopathy TXC009
Toxic Megacolon TXC001
Toxic Myocarditis TXC010
Toxic Oil Syndrome TXC020
Toxic Optic Neuropathy TXC008
Toxic Pneumonitis TXC007
Toxic Shock Syndrome TXC005
Toxicity or Absent Response to Clozapine TXC021
Toxicodendron Dermatitis TXC003
Toxocariasis TXC011
Toxoplasmosis TXP001
Tp63-Related Disorders TP6001
Tpm1-Related Dilated Cardiomyopathy TPM001
Tpm1-Related Familial Hypertrophic Cardiomyopathy TPM002
Tpm2-Related Arthrogryposis Multiplex Congenita, Distal, Type 2b TPM003
Tpm2-Related Congenital Fiber-Type Disproportion TPM007
Tpm2-Related Nemaline Myopathy TPM004
Tpm3-Related Congenital Fiber-Type Disproportion TPM005
Tpm3-Related Nemaline Myopathy TPM006
Tpmt-Related Altered Drug Metabolism TPM008
Traboulsi Syndrome TRB005
Trachea Adenoid Cystic Carcinoma TRC014
Trachea Leiomyoma TRC001
Trachea Squamous Cell Carcinoma TRC017
Tracheal Agenesis TRC035
Tracheal Calcification TRC016
Tracheal Cancer TRC025
Tracheal Disease TRC026
Tracheal Lymphoma TRC018
Tracheal Stenosis TRC005
Tracheitis TRC020
Tracheoesophageal Fistula TRC040
Tracheomalacia TRC097
Tracheopathia Osteoplastica TRC115
Trachoma TRC008
Transaldolase Deficiency TRN021
Transcobalamin Deficiency TRN059
Transcobalamin I Deficiency TRN067
Transcobalamin Ii Deficiency TRN022
Transient Arthritis TRN014
Transient Bullous of the Newborn TRN023
Transient Cerebral Ischemia TRN015
Transient Erythroblastopenia of Childhood TRN030
Transient Global Amnesia TRN012
Transient Hypogammaglobulinemia TRN016
Transient Hypogammaglobulinemia of Infancy TRN009
Transient Neonatal Neutropenia TRN017
Transient Neonatal Thrombocytopenia TRN013
Transient Refractive Change TRN011
Transient Tic Disorder TRN005
Transitional Cell Carcinoma TRN018
Transitional Meningioma TRN002
Transitional Papilloma TRN019
Transposition of Great Arteries, Dextro-Looped 3 TRN035
Transposition of the Great Arteries TRN044
Transposition of the Great Arteries, Dextro-Looped 1 TRN038
Transposition of the Great Arteries, Dextro-Looped 2 TRN036
Transsexualism TRN007
Transverse Colon Cancer TRN003
Transverse Myelitis TRN034
Transvestism TRN006
Traumatic Brain Injury TRM010
Traumatic Glaucoma TRM002
Trdn-Related Catecholaminergic Polymorphic Ventricular Tachycardia TRD007
Treacher Collins Syndrome 1 TRC072
Treacher Collins Syndrome 2 TRC073
Treacher Collins Syndrome 3 TRC071
Trehalase Deficiency TRH001
Trem2-Related Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy TRM008
Tremor TRM003
Tremor, Hereditary Essential, 2 TRM020
Tremor, Hereditary Essential, 3 TRM016
Tremor, Hereditary Essential, 4 TRM017
Trench Fever TRN004
Trichilemmal Cyst 1 TRC069
Trichinosis TRC023
Trichodontoosseous Syndrome TRC029
Trichoepithelioma, Multiple Familial, 1 TRC095
Trichoepithelioma, Multiple Familial, 2 TRC094
Trichohepatoenteric Syndrome 1 TRC086
Trichohepatoenteric Syndrome 2 TRC078
Trichomegaly TRC077
Trichomoniasis TRC003
Trichorhinophalangeal Syndrome Type 1 and 3 TRC104
Trichorhinophalangeal Syndrome, Type I TRC092
Trichorhinophalangeal Syndrome, Type Ii TRC091
Trichorhinophalangeal Syndrome, Type Iii TRC093
Trichosporonosis TRC006
Trichostrongyloidiasis TRC027
Trichostrongylosis TRC013
Trichothiodystrophy 1, Photosensitive TRC102
Trichothiodystrophy 2, Photosensitive TRC099
Trichothiodystrophy 3, Photosensitive TRC100
Trichothiodystrophy 4, Nonphotosensitive TRC101
Trichothiodystrophy 5, Nonphotosensitive TRC103
Trichotillomania TRC010
Trichuriasis TRC012
Tricuspid Atresia TRC062
Tricuspid Valve Disease TRC087
Tricuspid Valve Insufficiency TRC022
Tricuspid Valve Prolapse TRC007
Tricuspid Valve Stenosis TRC021
Trifunctional Protein Deficiency TRF001
Trigeminal Nerve Disease TRG003
Trigeminal Neuralgia TRG002
Trigonitis TRG001
Trigonocephaly 1 TRG016
Trigonocephaly 2 TRG015
Trigonocephaly, Nonsyndromic TRG011
Trim32-Related Bardet-Biedl Syndrome TRM009
Trimethylaminuria TRM004
Triphalangeal Thumb TRP015
Triple X Syndrome TRP009
Triple-Receptor Negative Breast Cancer TRP003
Triploidy TRP014
Trismus-Pseudocamptodactyly Syndrome TRS007
Trisomy 22 TRS012
Trophoblastic Neoplasm TRP005
Tropical Calcific Pancreatitis TRP008
Tropical Endomyocardial Fibrosis TRP020
Tropical Spastic Paraparesis TRP002
Tropical Sprue TRP004
Troyer Syndrome TRY002
Trpv4-Associated Disorders TRP021
Trypanosomiasis TRY001
Trypsinogen Deficiency TRY003
Tryptophan Hydroxylase Deficiency TRY007
Tsc1-Related Lymphangioleiomyomatosis TSC002
Tsc2 Angiomyolipomas, Renal, Modifier of TSC001
Tsen2-Related Pontocerebellar Hypoplasia TSN001
Tsen34-Related Pontocerebellar Hypoplasia TSN002
Tsen54-Related Pontocerebellar Hypoplasia TSN003
Tsh Producing Pituitary Tumor TSH001
Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant TSP001
Ttc21b-Related Joubert Syndrome TTC001
Ttc8-Related Bardet-Biedl Syndrome TTC002
Ttc8-Related Retinitis Pigmentosa TTC003
Ttn-Related Dilated Cardiomyopathy TTN004
Ttn-Related Familial Hypertrophic Cardiomyopathy TTN005
Tubb3-Related Congenital Fibrosis of the Extraocular Muscles TBB003
Tuberculoid Leprosy TBR006
Tuberculosis TBR010
Tuberculous Empyema TBR009
Tuberculous Epididymitis TBR003
Tuberculous Meningitis TBR011
Tuberculous Peritonitis TBR008
Tuberculous Salpingitis TBR002
Tuberculum Sellae Meningioma TBR007
Tuberous Sclerosis TBR001
Tuberous Sclerosis-1 TBR024
Tubular Adenocarcinoma TBL003
Tubulinopathies TBL023
Tubulocystic Carcinoma TBL016
Tufting Enteropathy TFT003
Tukel Syndrome TKL001
Tularemia TLR001
Tulp1-Related Leber Congenital Amaurosis TLP003
Tulp1-Related Retinitis Pigmentosa TLP004
Tumor of Exocrine Pancreas TMR001
Tumor Predisposition Syndrome TMR010
Tumoral Calcinosis, Familial, Normophosphatemic TMR012
Tumoral Calcinosis, Hyperphosphatemic, Familial TMR011
Tungiasis TNG001
Turner Syndrome TRN020
Twin-to-Twin Transfusion Syndrome TWN001
Twist1-Related Craniosynostosis TWS001
Tylosis with Esophageal Cancer TYL002
Tympanic Membrane Disease TYM002
Tympanosclerosis TYM001
Type 2a Von Willebrand Disease TYP014
Type 2b Von Willebrand Disease TYP015
Type 2m Von Willebrand Disease TYP016
Type 2n Von Willebrand Disease TYP017
Type C Thymoma TYP010
Type Ii Collagenopathies TYP019
Type Ii Mixed Cryoglobulinemia TYP024
Typhoid Fever TYP007
Typhoidal Tularemia TYP004
Typhus TYP011
Typical Congenital Nemaline Myopathy TYP026
Typical Urticaria Pigmentosa TYP022
Tyrobp-Related Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy TYR007
Tyrosine Hydroxylase-Deficient Dopa-Responsive Dystonia TYR008
Tyrosinemia TYR004
Tyrosinemia, Type I TYR012
Tyrosinemia, Type Ii TYR013
Tyrosinemia, Type Iii TYR011