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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Transcobalamin deficiency

ORPHA:859Ауру
Autosomal recessive

Transgrediens et progrediens palmoplantar keratoderma

ORPHA:495Ауру

Transient erythroblastopenia of childhood

ORPHA:98871Ауру

Transient familial neonatal hyperbilirubinemia

ORPHA:2312Ауру

Transient hyperammonemia of the newborn

ORPHA:289877Жағдай

Transient infantile hypertriglyceridemia and hepatosteatosis

ORPHA:300293Ауру
Autosomal recessive

Transient myeloproliferative syndrome

ORPHA:420611Ауру
Not applicable

Transient neonatal diabetes mellitus

ORPHA:99886Ауру
Autosomal dominant, Autosomal recessive, Not applicable

Transient neonatal multiple acyl-CoA dehydrogenase deficiency

ORPHA:329942Ауру
Autosomal dominant

Transient neonatal myasthenia gravis

ORPHA:391504Клин. под.
Not applicable

Transient predisposition to invasive pyogenic bacterial infection

ORPHA:70592Ауру
Autosomal recessive

Transient pseudohypoaldosteronism

ORPHA:93164Ауру
Not applicable

Transient tyrosinemia of the newborn

ORPHA:3402Ауру

Transitional cell carcinoma of the corpus uteri

ORPHA:213746Ауру

Transketolase deficiency

ORPHA:488618Мальф.
Autosomal recessive

Transposition of the great arteries

ORPHA:216675Сан.
Multigenic/multifactorial, Not applicable

Treacher-Collins syndrome

ORPHA:861Мальф.
Autosomal dominant, Autosomal recessive

Trehalase deficiency

ORPHA:103909Ауру
Autosomal dominant

Tremor-ataxia-central hypomyelination syndrome

ORPHA:447896Клин. под.
Autosomal recessive

Tremor-nystagmus-duodenal ulcer syndrome

ORPHA:3350Ауру

Trench fever

ORPHA:64694Ауру

Trichinellosis

ORPHA:863Ауру
Not applicable

Tricho-dento-osseous syndrome

ORPHA:3352Мальф.
Autosomal dominant

Tricho-retino-dento-digital syndrome

ORPHA:1264Мальф.
Autosomal dominant