MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Follicular dendritic cell sarcoma

ORPHA:86902Заболевание

Follicular lymphoma

ORPHA:545Заболевание
Multigenic/multifactorial, Not applicable

Folliculotropic mycosis fungoides

ORPHA:178512Заболевание
Not applicable

Fontan-associated liver disease

ORPHA:699068Заболевание
Not applicable

Foodborne botulism

ORPHA:228371Клин. подтип

Formiminoglutamic aciduria

ORPHA:51208Заболевание
Autosomal recessive

Fountain syndrome

ORPHA:3219Мальформация
Autosomal recessive

Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome

ORPHA:397618Заболевание
Autosomal recessive

Foveal hypoplasia-presenile cataract syndrome

ORPHA:2253Заболевание
Autosomal dominant

Fowler urethral sphincter dysfunction syndrome

ORPHA:2795Заболевание
Unknown

Fowler vasculopathy

ORPHA:221126Мальформация
Autosomal recessive

Fragile X syndrome

ORPHA:908Мальформация
X-linked dominant

Fragile X-associated primary ovarian insufficiency

ORPHA:642691Заболевание

Fragile X-associated tremor/ataxia syndrome

ORPHA:93256Мальформация
X-linked dominant

Frank-Ter Haar syndrome

ORPHA:137834Заболевание
Autosomal recessive

Fraser syndrome

ORPHA:2052Мальформация
Autosomal recessive

Frasier syndrome

ORPHA:347Заболевание
Autosomal dominant

Free sialic acid storage disease

ORPHA:834Заболевание
Autosomal recessive

Free sialic acid storage disease, infantile form

ORPHA:309324Клин. подтип
Autosomal recessive

Freeman-Sheldon syndrome

ORPHA:2053Мальформация
Autosomal dominant, Autosomal recessive

Frey syndrome

ORPHA:662240Clinical syndrome
Not applicable

Fried syndrome

ORPHA:85335Мальформация
X-linked recessive

Fried's tooth and nail syndrome

ORPHA:99672Мальформация

Friedreich ataxia

ORPHA:95Заболевание
Autosomal recessive