Genetic Conditions

Betterchem

Health Drug Information DMFs Portal 21CFR Search Site Map

Genetic Conditions…

[Index] | [Continue]

Tay-Sachs disease

TD with straight femurs and cloverleaf skull see thanatophoric dysplasia, type 2

Telangiectasia, cerebello-oculocutaneous see ataxia-telangiectasia

Testicular feminization syndrome see androgen insensitivity syndrome

tetrahydrobiopterin deficiency

TFM see androgen insensitivity syndrome

TFP deficiency see mitochondrial trifunctional protein deficiency

thalassemia intermedia see beta thalassemia

Thalassemia Major see beta thalassemia

thanatophoric dysplasia

Thrombophilia due to deficiency of cofactor for activated protein C, Leiden type see factor V Leiden thrombophilia

Thyroid Cancer see multiple endocrine neoplasia type 2

Thyroid Diseases

TMAU see trimethylaminuria

tomaculous neuropathy see hereditary neuropathy with liability to pressure palsies

Total HPRT deficiency see Lesch-Nyhan syndrome

Total hypoxanthine-guanine phosphoribosyl transferase deficiency see Lesch-Nyhan syndrome

TPA deficiency see mitochondrial trifunctional protein deficiency

Transmissible Dementias see prion disease

Transmissible Spongiform Encephalopathies see prion disease

Trias fragilitis ossium see osteogenesis imperfecta, type I

trifunctional protein deficiency, type 1 see long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

trifunctional protein deficiency, type 2 see mitochondrial trifunctional protein deficiency

trimethylaminuria

triple X syndrome

Triplo X syndrome see triple X syndrome

Trisomy 16-18 see Edwards syndrome

Trisomy 21 see Down syndrome

Trisomy E syndrome see Edwards syndrome

Trisomy 13 syndrome see Patau syndrome

Trisomy 18 syndrome see Edwards syndrome

Trisomy X see triple X syndrome

Troisier-Hanot-Chauffard syndrome see hemochromatosis

TS see Turner syndrome

TSD see Tay-Sachs disease

TSEs see prion disease

tuberose sclerosis see tuberous sclerosis

tuberous sclerosis

Turner-like syndrome see Noonan syndrome

Turner syndrome

Turner syndrome in female with X chromosome see Noonan syndrome

Turner's phenotype, karyotype normal see Noonan syndrome

Turner's Syndrome see Turner syndrome

Type 2 Gaucher Disease see Gaucher disease, type 2

Type 3 Gaucher Disease see Gaucher disease, type 3