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Rare conditions starting with T
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220 conditions starting with T
- T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta
- T-B+ severe combined immunodeficiency due to CD45 deficiency
- T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
- T-B+ severe combined immunodeficiency due to JAK3 deficiency
- T-cell and NK-cell neoplasm
- T-cell childhood acute lymphocytic leukemia
- T-cell immunodeficiency with epidermodysplasia verruciformis
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- T-cell large granular lymphocyte leukemia
- T-cell prolymphocytic leukemia
- T-cell/histiocyte rich large B cell lymphoma
- T-lymphocyte deficiency
- Tabes dorsalis
- Takayasu arteritis
- Takotsubo cardiomyopathy
- Tall stature-intellectual disability-renal anomalies syndrome
- Tall stature-scoliosis-macrodactyly of the great toes syndrome
- Talo-patello-scaphoid osteolysis
- Tangier disease
- TARP syndrome
- Tarsal kink syndrome
- Tarsal tunnel syndrome
- Tarsal-carpal coalition syndrome
- Tatton-Brown-Rahman overgrowth syndrome
- Taurodontia-absent teeth-sparse hair syndrome
- Tay-Sachs disease
- Tay-Sachs disease, variant AB
- Taybi-linder syndrome
- TCR-alpha-beta-positive T-cell deficiency
- Teebi hypertelorism syndrome 1
- Teebi-Shaltout syndrome
- Tel Hashomer camptodactyly syndrome
- Telangiectasia, hereditary hemorrhagic, type 2
- Telecanthus-hypertelorism-strabismus-pes cavus syndrome
- TELO2-related intellectual disability-neurodevelopmental disorder
- Tempi syndrome
- Temple syndrome
- Temple-Baraitser syndrome
- Temporal arteritis
- Temporal lobe epilepsy
- Temtamy preaxial brachydactyly syndrome
- Temtamy syndrome
- Tenosynovial giant cell tumor, diffuse type
- Teratoma with malignant transformation
- Terminal osseous dysplasia-pigmentary defects syndrome
- Tessier number 4 facial cleft
- Tessier number 5 facial cleft
- Tessier number 6 facial cleft
- Testicular agenesis
- Testicular seminoma
- Testosterone 17-beta-dehydrogenase deficiency
- Tetanus
- Tetraamelia
- Tetraamelia-multiple malformations syndrome
- Tetragametic chimerism
- Tetralogy of Fallot
- Tetramelic monodactyly
- Tetraploidy syndrome
- Tetrasomy 18p
- Tetrasomy 21
- Tetrasomy 5p
- Tetrasomy 9p
- TFRC-related combined immunodeficiency
- Thakker-Donnai syndrome
- Thalassemia
- Thanatophoric dysplasia
- Thanatophoric dysplasia type 1
- Thanatophoric dysplasia, type 2
- Thickened earlobes-conductive deafness syndrome
- Thiel-Behnke corneal dystrophy
- Thin ribs-tubular bones-dysmorphism syndrome
- Thiopurine S-methyltransferase deficiency
- THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
- Thomas syndrome
- Thomsen and Becker disease
- Thong Douglas Ferrante syndrome
- Thoracic dysplasia-hydrocephalus syndrome
- Thoraco-abdominal enteric duplication
- Thoracomelic dysplasia
- Thromboangiitis obliterans
- Thrombocytopenia 1
- Thrombocytopenia 2
- Thrombocytopenia 6
- Thrombocytopenia with congenital dyserythropoietic anemia
- Thrombomodulin-related bleeding disorder
- Thrombophilia due to protein C deficiency, autosomal recessive
- Thrombophilia due to thrombin defect
- Thrombotic thrombocytopenic purpura
- Thumb deformity-alopecia-pigmentation anomaly syndrome
- Thumb stiffness-brachydactyly-intellectual disability syndrome
- Thymic epithelial neoplasm
- Thymic-renal-anal-lung dysplasia
- Thymus cancer
- Thyrocerebrorenal syndrome
- Thyroid agenesis
- Thyroid cancer, nonmedullary, 2
- Thyroid gland undifferentiated (anaplastic) carcinoma
- Thyroid hemiagenesis
- Thyroid hormone metabolism, abnormal 1
- Thyroid hypoplasia
- Thyrotoxic periodic paralysis
- Tibia vara
- Tibia, hypoplasia or aplasia of, with polydactyly
- Tibial aplasia-ectrodactyly syndrome
- Tibial hemimelia
- Tibial muscular dystrophy
- Tibio-fibular synostosis
- Tick paralysis
- Tick-borne encephalitis
- Tietz syndrome
- Timothy syndrome
- TMEM165-congenital disorder of glycosylation
- TMEM199-CDG
- TNF receptor-associated periodic fever syndrome (TRAPS)
- Tolosa-Hunt syndrome
- Toluene embryopathy
- Toriello-Carey syndrome
- Toriello-Lacassie-Droste syndrome
- Torsade-de-pointes syndrome with short coupling interval
- Torsion dystonia 13
- Torsion dystonia 17
- Torsion dystonia 2
- Torsion dystonia 4
- Torsion dystonia 6
- Torticollis
- Torticollis-keloids-cryptorchidism-renal dysplasia syndrome
- Townes syndrome
- Toxic shock syndrome
- Toxocariasis
- Tracheal agenesis
- Tracheobroncheopathia osteoplastica
- TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome
- Transcobalamin I deficiency
- Transcobalamin II deficiency
- Transgrediens et progrediens palmoplantar keratoderma
- Transient bullous dermolysis of the newborn
- Transient erythroblastopenia of childhood
- Transient hypogammaglobulinemia of infancy
- Transient infantile hypertriglyceridemia and hepatosteatosis
- Transient myeloproliferative syndrome
- Transient neonatal multiple acyl-CoA dehydrogenase deficiency
- Transient tyrosinemia of the newborn
- Transitional cell carcinoma
- Transketolase deficiency
- Transposition of the great arteries
- Treacher Collins syndrome
- Treacher Collins syndrome 3
- Trench fever
- Triatrial heart
- Tricho-dento-osseous syndrome
- Tricho-oculo-dermo-vertebral syndrome
- Trichodental syndrome
- Trichodermodysplasia-dental alterations syndrome
- Trichodysplasia-amelogenesis imperfecta syndrome
- Trichodysplasia-xeroderma syndrome
- Trichofolliculoma
- Trichohepatoenteric syndrome
- Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
- Trichoodontoonychial dysplasia
- Trichorhinophalangeal dysplasia type I
- Trichorhinophalangeal syndrome
- Trichothiodystrophy
- Tricuspid atresia
- Trigeminal neuralgia
- Triglyceride storage disease with ichthyosis
- Trigonocephaly-bifid nose-acral anomalies syndrome
- Trigonocephaly-broad thumbs syndrome
- Trigonocephaly-short stature-developmental delay syndrome
- Triopia
- Triosephosphate isomerase deficiency
- Triphalangeal thumbs-brachyectrodactyly syndrome
- Triploidy
- Trisomy 10p
- Trisomy 12p
- Trisomy 17p
- Trisomy 18
- Trisomy 18p
- Trisomy 1q
- Trisomy 20p
- Trisomy 22
- Trisomy 4p
- Trisomy 5p
- Trisomy 6
- Trisomy 8p
- Trisomy 8q
- Trisomy X syndrome
- Troyer syndrome
- True unicornuate uterus
- Tryptophan malabsorption syndrome
- Tuberculosis
- Tuberculosis of meninges
- Tuberous sclerosis syndrome
- Tubular duplication of the esophagus
- Tubular renal disease-cardiomyopathy syndrome
- Tubulinopathy-associated dysgyria
- Tubulointerstitial kidney disease, autosomal dominant, 2
- Tubulointerstitial nephritis and uveitis syndrome
- Tufted angioma of skin
- Tukel syndrome
- Tularemia
- Tumor predisposition syndrome 3
- Tumor-induced osteomalacia
- Tungiasis
- Turcot syndrome
- Turner syndrome
- Twin-to-twin transfusion
- Tympanic paraganglioma
- Type A2 brachydactyly
- Type A5 brachydactyly
- Type I complement component 8 deficiency
- Type II complement component 8 deficiency
- Type IV short rib polydactyly syndrome
- Typhoid fever
- Typical nemaline myopathy
- Tyrosinase-positive oculocutaneous albinism
- Tyrosine hydroxylase deficiency
- Tyrosinemia
- Tyrosinemia type I
- Tyrosinemia type II
- Tyrosinemia type III
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