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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Fever-associated acute infantile liver failure syndrome

ORPHA:464724Disease
Autosomal recessive

Fibrillary astrocytoma

ORPHA:251601Hist. sub.

Fibroblastic rheumatism

ORPHA:477650Disease

Fibrochondrogenesis

ORPHA:2021Disease
Autosomal dominant, Autosomal recessive

Fibrodysplasia ossificans progressiva

ORPHA:337Disease
Autosomal dominant, Not applicable

Fibrohistiocytic inflammatory pseudotumor of the liver

ORPHA:555434Clin. sub.

Fibrolamellar hepatocellular carcinoma

ORPHA:401920Disease
Not applicable

Fibromuscular dysplasia of the arteries of the extremities

ORPHA:698069Clin. sub.
Not applicable

Fibromuscular dysplasia of the cervical and intracranial arteries

ORPHA:698036Clin. sub.
Not applicable

Fibromuscular dysplasia of the coronary arteries

ORPHA:698059Clin. sub.
Not applicable

Fibromuscular dysplasia of the renal arteries

ORPHA:698043Clin. sub.
Not applicable

Fibromuscular dysplasia of the visceral arteries

ORPHA:698063Clin. sub.
Not applicable

Fibronectin glomerulopathy

ORPHA:84090Disease
Autosomal dominant

Fibrosarcoma

ORPHA:2030Disease
Not applicable

Fibrosis-neurodegeneration-cerebral angiomatosis syndrome

ORPHA:621758Disease

Fibrotic hypersensitivity pneumonitis

ORPHA:686465Clin. sub.
Not applicable

Fibrous dysplasia of bone

ORPHA:249Malform.
Not applicable

Fibular aplasia-complex brachydactyly syndrome

ORPHA:2639Malform.
Autosomal recessive

Fibular aplasia-ectrodactyly syndrome

ORPHA:1118Malform.
Autosomal dominant

Fibular dimelia-diplopodia syndrome

ORPHA:1757Malform.
Not applicable

Fibulo-ulnar hypoplasia-renal anomalies syndrome

ORPHA:2256Malform.

Filariasis

ORPHA:2034Cat.
Not applicable

Filippi syndrome

ORPHA:3255Malform.
Autosomal recessive

Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome

ORPHA:369979Malform.