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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы
Найдено 3,968 заболеваний (Disease) Сброс

Bullous impetigo

ORPHA:36237Disease
Not applicable

Bullous lichen planus

ORPHA:33408Disease
Autosomal dominant, Not applicable

Bullous pemphigoid

ORPHA:703Disease
Not applicable

Burkitt lymphoma

ORPHA:543Disease
Not applicable

Burning mouth syndrome

ORPHA:353253Disease

Butterfly-shaped pigment dystrophy

ORPHA:99001Disease
Autosomal dominant

C11ORF73-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:495844Disease
Autosomal recessive

CACH syndrome

ORPHA:135Disease
Autosomal recessive

CAD-CDG

ORPHA:448010Disease
Autosomal recessive

CADDS

ORPHA:369942Disease
X-linked recessive

CADINS disease

ORPHA:619972Disease
Autosomal dominant

CANOMAD syndrome

ORPHA:71279Disease

CARD8-related inflammatory bowel disease

ORPHA:714410Disease
Autosomal dominant

CCDC115-CDG

ORPHA:468684Disease
Autosomal recessive

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

ORPHA:600668Disease
Autosomal dominant

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

ORPHA:646278Disease
Autosomal dominant

CDKL5-deficiency disorder

ORPHA:505652Disease
X-linked dominant

CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome

ORPHA:566067Disease
Autosomal recessive

CEDNIK syndrome

ORPHA:66631Disease
Autosomal recessive

CELSR1-related late-onset primary lymphedema

ORPHA:569816Disease
Autosomal dominant

CHD4-related neurodevelopmental disorder

ORPHA:653712Disease
Autosomal dominant

CHD8 overgrowth syndrome

ORPHA:642675Disease
Autosomal dominant

CHILD syndrome

ORPHA:139Disease
X-linked dominant

CHST3-related skeletal dysplasia

ORPHA:263463Disease
Autosomal recessive