MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Transcobalamin deficiency

ORPHA:859Заболевание
Autosomal recessive

Transgrediens et progrediens palmoplantar keratoderma

ORPHA:495Заболевание

Transient erythroblastopenia of childhood

ORPHA:98871Заболевание

Transient familial neonatal hyperbilirubinemia

ORPHA:2312Заболевание

Transient hyperammonemia of the newborn

ORPHA:289877Особая клин. ситуация

Transient infantile hypertriglyceridemia and hepatosteatosis

ORPHA:300293Заболевание
Autosomal recessive

Transient myeloproliferative syndrome

ORPHA:420611Заболевание
Not applicable

Transient neonatal diabetes mellitus

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

Transient neonatal multiple acyl-CoA dehydrogenase deficiency

ORPHA:329942Заболевание
Autosomal dominant

Transient neonatal myasthenia gravis

ORPHA:391504Клин. подтип
Not applicable

Transient predisposition to invasive pyogenic bacterial infection

ORPHA:70592Заболевание
Autosomal recessive

Transient pseudohypoaldosteronism

ORPHA:93164Заболевание
Not applicable

Transient tyrosinemia of the newborn

ORPHA:3402Заболевание

Transitional cell carcinoma of the corpus uteri

ORPHA:213746Заболевание

Transketolase deficiency

ORPHA:488618Мальформация
Autosomal recessive

Transposition of the great arteries

ORPHA:216675Категория
Multigenic/multifactorial, Not applicable

Treacher-Collins syndrome

ORPHA:861Мальформация
Autosomal dominant, Autosomal recessive

Trehalase deficiency

ORPHA:103909Заболевание
Autosomal dominant

Tremor-ataxia-central hypomyelination syndrome

ORPHA:447896Клин. подтип
Autosomal recessive

Tremor-nystagmus-duodenal ulcer syndrome

ORPHA:3350Заболевание

Trench fever

ORPHA:64694Заболевание

Trichinellosis

ORPHA:863Заболевание
Not applicable

Tricho-dento-osseous syndrome

ORPHA:3352Мальформация
Autosomal dominant

Tricho-retino-dento-digital syndrome

ORPHA:1264Мальформация
Autosomal dominant