MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Fever-associated acute infantile liver failure syndrome

ORPHA:464724Заболевание
Autosomal recessive

Fibrillary astrocytoma

ORPHA:251601Гист. подтип

Fibroblastic rheumatism

ORPHA:477650Заболевание

Fibrochondrogenesis

ORPHA:2021Заболевание
Autosomal dominant, Autosomal recessive

Fibrodysplasia ossificans progressiva

ORPHA:337Заболевание
Autosomal dominant, Not applicable

Fibrohistiocytic inflammatory pseudotumor of the liver

ORPHA:555434Клин. подтип

Fibrolamellar hepatocellular carcinoma

ORPHA:401920Заболевание
Not applicable

Fibromuscular dysplasia of the arteries of the extremities

ORPHA:698069Клин. подтип
Not applicable

Fibromuscular dysplasia of the cervical and intracranial arteries

ORPHA:698036Клин. подтип
Not applicable

Fibromuscular dysplasia of the coronary arteries

ORPHA:698059Клин. подтип
Not applicable

Fibromuscular dysplasia of the renal arteries

ORPHA:698043Клин. подтип
Not applicable

Fibromuscular dysplasia of the visceral arteries

ORPHA:698063Клин. подтип
Not applicable

Fibronectin glomerulopathy

ORPHA:84090Заболевание
Autosomal dominant

Fibrosarcoma

ORPHA:2030Заболевание
Not applicable

Fibrosis-neurodegeneration-cerebral angiomatosis syndrome

ORPHA:621758Заболевание

Fibrotic hypersensitivity pneumonitis

ORPHA:686465Клин. подтип
Not applicable

Fibrous dysplasia of bone

ORPHA:249Мальформация
Not applicable

Fibular aplasia-complex brachydactyly syndrome

ORPHA:2639Мальформация
Autosomal recessive

Fibular aplasia-ectrodactyly syndrome

ORPHA:1118Мальформация
Autosomal dominant

Fibular dimelia-diplopodia syndrome

ORPHA:1757Мальформация
Not applicable

Fibulo-ulnar hypoplasia-renal anomalies syndrome

ORPHA:2256Мальформация

Filariasis

ORPHA:2034Категория
Not applicable

Filippi syndrome

ORPHA:3255Мальформация
Autosomal recessive

Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome

ORPHA:369979Мальформация