MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов
Найдено 3,968 заболеваний (Заболевание)Сбросить

Bullous impetigo

ORPHA:36237Заболевание
Not applicable

Bullous lichen planus

ORPHA:33408Заболевание
Autosomal dominant, Not applicable

Bullous pemphigoid

ORPHA:703Заболевание
Not applicable

Burkitt lymphoma

ORPHA:543Заболевание
Not applicable

Burning mouth syndrome

ORPHA:353253Заболевание

Butterfly-shaped pigment dystrophy

ORPHA:99001Заболевание
Autosomal dominant

C11ORF73-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:495844Заболевание
Autosomal recessive

CACH syndrome

ORPHA:135Заболевание
Autosomal recessive

CAD-CDG

ORPHA:448010Заболевание
Autosomal recessive

CADDS

ORPHA:369942Заболевание
X-linked recessive

CADINS disease

ORPHA:619972Заболевание
Autosomal dominant

CANOMAD syndrome

ORPHA:71279Заболевание

CARD8-related inflammatory bowel disease

ORPHA:714410Заболевание
Autosomal dominant

CCDC115-CDG

ORPHA:468684Заболевание
Autosomal recessive

CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome

ORPHA:600668Заболевание
Autosomal dominant

CDK13-related developmental delay-intellectual disability-facial dysmorphism-congenital heart defects syndrome

ORPHA:646278Заболевание
Autosomal dominant

CDKL5-deficiency disorder

ORPHA:505652Заболевание
X-linked dominant

CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome

ORPHA:566067Заболевание
Autosomal recessive

CEDNIK syndrome

ORPHA:66631Заболевание
Autosomal recessive

CELSR1-related late-onset primary lymphedema

ORPHA:569816Заболевание
Autosomal dominant

CHD4-related neurodevelopmental disorder

ORPHA:653712Заболевание
Autosomal dominant

CHD8 overgrowth syndrome

ORPHA:642675Заболевание
Autosomal dominant

CHILD syndrome

ORPHA:139Заболевание
X-linked dominant

CHST3-related skeletal dysplasia

ORPHA:263463Заболевание
Autosomal recessive