MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Brain arteriovenous malformation

ORPHA:46724Морф. аномалия
No data available

Brain dopamine-serotonin vesicular transport disease

ORPHA:352649Заболевание
Autosomal recessive

Brain malformation-congenital heart disease-postaxial polydactyly syndrome

ORPHA:75389Мальформация
Unknown

Brain-lung-thyroid syndrome

ORPHA:209905Заболевание
Autosomal dominant

Branchio-oculo-facial syndrome

ORPHA:1297Мальформация
Autosomal dominant

Branchiogenic deafness syndrome

ORPHA:50815Мальформация
Autosomal dominant

Branchiootic syndrome

ORPHA:52429Мальформация
Autosomal dominant

Branchioskeletogenital syndrome

ORPHA:1299Мальформация
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. группа
Not applicable

Bronchogenic cyst

ORPHA:2357Морф. аномалия
Unknown

Bronchopulmonary dysplasia

ORPHA:70589Мальформация
Not applicable

Brooke-Spiegler syndrome

ORPHA:79493Заболевание
Autosomal dominant

Brucellosis

ORPHA:1304Заболевание
Not applicable

Bruck syndrome

ORPHA:2771Мальформация
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. подтип
Not applicable

Bullous impetigo

ORPHA:36237Заболевание
Not applicable