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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Fever-associated acute infantile liver failure syndrome

ORPHA:464724Заболевание
Autosomal recessive

Fibrillary astrocytoma

ORPHA:251601Гист. подт.

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. подт.

Fibrolamellar hepatocellular carcinoma

ORPHA:401920Заболевание
Not applicable

Fibromuscular dysplasia of the arteries of the extremities

ORPHA:698069Клин. подт.
Not applicable

Fibromuscular dysplasia of the cervical and intracranial arteries

ORPHA:698036Клин. подт.
Not applicable

Fibromuscular dysplasia of the coronary arteries

ORPHA:698059Клин. подт.
Not applicable

Fibromuscular dysplasia of the renal arteries

ORPHA:698043Клин. подт.
Not applicable

Fibromuscular dysplasia of the visceral arteries

ORPHA:698063Клин. подт.
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. подт.
Not applicable

Fibrous dysplasia of bone

ORPHA:249Порок
Not applicable

Fibular aplasia-complex brachydactyly syndrome

ORPHA:2639Порок
Autosomal recessive

Fibular aplasia-ectrodactyly syndrome

ORPHA:1118Порок
Autosomal dominant

Fibular dimelia-diplopodia syndrome

ORPHA:1757Порок
Not applicable

Fibulo-ulnar hypoplasia-renal anomalies syndrome

ORPHA:2256Порок

Filariasis

ORPHA:2034Кат.
Not applicable

Filippi syndrome

ORPHA:3255Порок
Autosomal recessive

Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome

ORPHA:369979Порок