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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

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

Brain arteriovenous malformation

ORPHA:46724Морф.
No data available

Brain dopamine-serotonin vesicular transport disease

ORPHA:352649Заболевание
Autosomal recessive

Brain malformation-congenital heart disease-postaxial polydactyly syndrome

ORPHA:75389Порок
Unknown

Brain-lung-thyroid syndrome

ORPHA:209905Заболевание
Autosomal dominant

Branchio-oculo-facial syndrome

ORPHA:1297Порок
Autosomal dominant

Branchiogenic deafness syndrome

ORPHA:50815Порок
Autosomal dominant

Branchiootic syndrome

ORPHA:52429Порок
Autosomal dominant

Branchioskeletogenital syndrome

ORPHA:1299Порок
Autosomal recessive, X-linked dominant

Brazilian hemorrhagic fever

ORPHA:319239Заболевание

Breast implant-associated anaplastic large cell lymphoma

ORPHA:667662Заболевание
Not applicable

Brittle cornea syndrome

ORPHA:90354Заболевание
Autosomal recessive

Brody myopathy

ORPHA:53347Заболевание
Autosomal dominant, Autosomal recessive

Bronchial neuroendocrine tumor

ORPHA:97287Заболевание
Not applicable

Bronchiolitis obliterans

ORPHA:1303Клин. гр.
Not applicable

Bronchogenic cyst

ORPHA:2357Морф.
Unknown

Bronchopulmonary dysplasia

ORPHA:70589Порок
Not applicable

Brooke-Spiegler syndrome

ORPHA:79493Заболевание
Autosomal dominant

Brucellosis

ORPHA:1304Заболевание
Not applicable

Bruck syndrome

ORPHA:2771Порок
Autosomal recessive

Brugada syndrome

ORPHA:130Заболевание
Autosomal dominant, Not applicable

Budd-Chiari syndrome

ORPHA:131Заболевание
Multigenic/multifactorial

Buerger disease

ORPHA:36258Заболевание
Not applicable

Bullous diffuse cutaneous mastocytosis

ORPHA:280785Клин. подт.
Not applicable

Bullous impetigo

ORPHA:36237Заболевание
Not applicable