Type 2 Diabetes Mellitus |
Tangier Disease |
Tay Sachs Disease |
Thrombasthenia |
Tuberous Sclerosis |
Tumor, Gastrointestinal Stromal |
Thiamine responsive megaloblastic anemia syndrome |
Tomaculous neuropathy |
Timothy syndrome |
Telomeric 22q13 Monosomy Syndrome |
Tietz syndrome |
Trichorhinophalangeal Syndrome, Type I |
Tay Sachs Disease, AB Variant |
T-cell immunodeficiency, congenital alopecia and nail dystrophy |
Type 1 Diabetes Mellitus |
Thrombocytopenia |
Thyroid cancer, papillary |
Townes-Brocks syndrome |
Triosephosphate Isomerase Deficiency |
Trichothiodystrophy Syndrome |
Thyroid Hormone Resistance Syndrome |
Turcot syndrome |
Tricho-dento-osseous syndrome |
Trimethylaminuria |
Thiopurine S methyltranferase deficiency |
Thanatophoric dysplasia, type 2 |
Thrombocytopenia 1 |
Tropical Calcific Pancreatitis |
Tuberous Sclerosis 2 |
Thanatophoric Dysplasia, Type I |
Tumoral Calcinosis, Hyperphosphatemic, Familial |
Trifunctional Protein Deficiency With Myopathy And Neuropathy |
Trifunctional Protein Deficiency, Type 1 |
Thrombocytopenia chromosome breakage |
Ter Haar syndrome |
TARP syndrome |
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations |
Temple-Baraitser Syndrome |
Transaldolase Deficiency |
Thyroid Dyshormonogenesis 4 |
Transient bullous dermolysis of the newborn |
Thrombophilia due to Activated Protein C Resistance |
Thyroid Hormone Metabolism, Abnormal |
Temtamy preaxial brachydactyly syndrome |
Tyrosine Kinase 2 Deficiency |
Thyroid Hormone Resistance, Generalized, Autosomal Dominant |
Teebi syndrome |
Temtamy syndrome |
Thrombasthenia-Thrombocytopenia, Hereditary |
Thrombocytopenia 4 |
Tourette Syndrome |
Tachycardia, Ventricular |
Thyroid cancer, medullary |
Tn Syndrome |
Thyroid Dyshormonogenesis 3 |
Thyroid Dyshormonogenesis 5 |
Thrombophilia |
Tight skin contracture syndrome, lethal |
Thyroid Dyshormonogenesis 2A |
Total Hypotrichosis, Mari type |
Transposition of the Great Arteries, Dextro-Looped 1 |
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis |
Thyroid Hormone Resistance, Selective Pituitary |
Thyroid Dyshormonogenesis 6 |
Thyroid Dyshormonogenesis 1 |
Trichohepatoenteric Syndrome |
Trichorhinophalangeal Syndrome, Type III |
Tumoral Calcinosis, Normophosphatemic, Familial |
Tooth Agenesis, Selective, 3 |
Tooth Agenesis, Selective, X-Linked, 1 |
Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Recessive |
Three M Syndrome 1 |
Thrombophilia, X-Linked, Due To Factor Ix Defect |
Thrombophilia Due To Histidine-Rich Glycoprotein Deficiency |
Thrombophilia due to Thrombomodulin Defect |
Tuberous Sclerosis 1 |
Testicular Germ Cell Tumor |
Tetra-amelia autosomal recessive |
Thyroid Hormone Resistance, Generalized, Autosomal Recessive |
Trichotillomania |
Trigonocephaly, Nonsyndromic |
Tooth Agenesis, Selective, 4 |
Terminal Osseous Dysplasia and Pigmentary Defects |
Three M Syndrome 2 |
Truncus Arteriosus, Persistent |
Tuberculoses |
Trehalase Deficiency |
Thromboxane Synthetase Deficiency |
Thin-Basement-Membrane Nephropathy |
Thyroid cancer, Hurthle cell |
Tauopathies |
Toenail Dystrophy, Isolated |
Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant |
Thrombocytopenia 3 |
Thromboses |
Thromboses, Venous |
Thoracic Aortic Aneurysm |
Tufted angioma |
Tachycardia |
Thromboembolism |
Tyrosinemias |
Thrombocytoses |
Trichorrhexis nodosa syndrome |
Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator |
Thrombophilia Due To Elevated Histidine-Rich Glycoprotein |
Trisomy Xq28 |
Tremors |
Telangiectasis, Retinal |
Tay-Sachs Disease, Variant B1 |
Teratoma |
Thyrotoxicoses |
Tuberculosis, Pulmonary |
Turner Syndrome |
Triphalangeal Thumb |
Thumb hypoplastic |
Tibia, Hypoplasia of, with Polydactyly |
Thrombophilia, hereditary |
Thymoma |
Telangiectasis |
Thyroid cancer, follicular |
Trypanosomiases |
Typhoid Fever |
Treatment-Resistant Depressive Disorders |
Teratoid Tumor, Atypical |
Tic Disorders |
Tibia, absence of |
Transient Myeloproliferative Disorder of Down Syndrome |
Taste Disorder |
Tetanies |
Tinnitus |
Toothache |
Torticollis |
Trichuriasis |
Trismus |
Trisomies |
Tick-Borne Diseases |
T-Lymphocytopenia, Idiopathic CD4-Positive |
Teratogenesis |
Typhlitis |
Tics |
Teratozoospermia |
Thumb deformity |
Thymic epithelial tumor |
Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum |
Thyrotropin, Biologically Inactive |
Tremor hereditary essential, 1 |
Thyrotropin-Releasing Hormone Resistance, Generalized |
Townes-Brocks-Branchiootorenal-Like Syndrome |
Thyroid Carcinoma With Thyrotoxicosis |
Torsion dystonia 7 |
Tooth Agenesis, Selective, 6 |
Tetraamelia multiple malformations |
T cell immunodeficiency primary |
T-Lymphocytopenia |
Thumb absent or hypoplastic |
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive |
Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant |
Trifunctional Protein Deficiency, Type 2 |
Thyrotropin deficiency, isolated |
Thromboangiitis Obliterans |
Tissue Adhesion |
Temporomandibular Joint Dysfunction Syndrome |
Thalassemia |
Thymus Hyperplasia |
Thyroiditides |
Toxoplasmoses |
Trichinellosis |
Trichostrongyloidiases |
Tympanic Membrane Perforation |
Teratoma, Ovarian |
Tukel syndrome |
Taurodontism |
Thymic aplasia |
Talipes Cavus |
Thyroid Adenoma, Hyperfunctioning |
Tarsal Coalition |
Tay-Sachs Disease, Juvenile |
Temperament |
Thinness |
Thrombophlebitides |
Thyroid Crisis |
Tooth, Supernumerary |
Tooth, Unerupted |
Toxemia |
Torticollis, congenital |
Trigger Finger Disorder |
Tuberculosis, Multidrug-Resistant |
Trichiases |
Tachypneas |
Testicular regression syndrome |
Tracheobronchomalacia |
Transcobalamin I Deficiency |
Telecanthus |
Tracheomalacia |
Talipes |
Tendinopathies |
Tuberculoses, Latent |
Thrombocytopenia, X-Linked, Intermittent |
Testicular Microlithiasis |
Tooth Agenesis, Selective, With Orofacial Cleft |
Taste Perceptions |
Thrombotic thrombocytopenic purpura, acquired |
TDP 43 Proteinopathies |
Tsc2 Angiomyolipomas, Renal, Modifier Of |
Temporomandibular ankylosis |
Trisomy 18 Syndrome |
Tooth Loss |
Tinea |
Tuberculous Peritonitis |
Teratocarcinoma |
Thyroxine-Binding Globulin Deficiency |
Temporal epilepsy, familial |
Tuberculosis, Central Nervous System |
Tubulointerstitial nephritis and uveitis |
Thyroid hormone plasma membrane transport defect |
Thecoma |
Tonsillitides |
Trachoma |
Toxoplasmoses, Cerebral |
Triple X syndrome |
Triploidy |
Tenosynovitides |
Trichomonas Infection |
Trophoblastic Neoplasms |
Tularemia |
Trophoblastic Tumor, Placental Site |
Transient erythroblastopenia of childhood |
Tuberculoses, Extensively Drug-Resistant |
Tabes Dorsalis |
Tachycardia, Atrioventricular Nodal Reentry |
Taeniases |
Tetanus |
Tietze Syndrome |
Tinea Capitis |
Tinea Pedis |
Tinea Versicolor |
Tuberculoma |
Tuberculosis, Gastrointestinal |
Trigeminal Nerve Disease |
Teratoma, Testicular |
Tetrasomy X |
Thrombocytopenia, cyclic |
Tungiasis |
Trichofolliculoma |
Telangiectasia, Hereditary Benign |
Tooth Agenesis, Selective, 5 |
Trichilemmal Cyst 1 |
Tooth Agenesis, Selective, 2 |
Thrombocytopenia Robin sequence |
Torulopsis |
Trauma and Stressor Related Disorders |
Trisomy 13 Syndrome |
T Lymphocytes |
Tendon |
Testis |
Thalamus |
Thumb |
Tibia |
Tidal Volume |
Tissue |
Toe |
Tongue |
Tooth |
Trachea |
Transport Vesicle |
Temperatures, Hot |
Teratoid Rhabdoid Tumor |