MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Bullous impetigo

ORPHA:36237Kr.
Not applicable

Bullous lichen planus

ORPHA:33408Kr.
Autosomal dominant, Not applicable

Bullous pemphigoid

ORPHA:703Kr.
Not applicable

Burkitt lymphoma

ORPHA:543Kr.
Not applicable

Burning mouth syndrome

ORPHA:353253Kr.

Butterfly-shaped pigment dystrophy

ORPHA:99001Kr.
Autosomal dominant

C11ORF73-related autosomal recessive hypomyelinating leukodystrophy

ORPHA:495844Kr.
Autosomal recessive

CACH syndrome

ORPHA:135Kr.
Autosomal recessive

CAD-CDG

ORPHA:448010Kr.
Autosomal recessive

CADDS

ORPHA:369942Kr.
X-linked recessive

CADINS disease

ORPHA:619972Kr.
Autosomal dominant

CANOMAD syndrome

ORPHA:71279Kr.

CARD8-related inflammatory bowel disease

ORPHA:714410Kr.
Autosomal dominant

CCDC115-CDG

ORPHA:468684Kr.
Autosomal recessive

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

ORPHA:600668Kr.
Autosomal dominant

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

ORPHA:646278Kr.
Autosomal dominant

CDKL5-deficiency disorder

ORPHA:505652Kr.
X-linked dominant

CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome

ORPHA:566067Kr.
Autosomal recessive

CEDNIK syndrome

ORPHA:66631Kr.
Autosomal recessive

CELSR1-related late-onset primary lymphedema

ORPHA:569816Kr.
Autosomal dominant

CHD4-related neurodevelopmental disorder

ORPHA:653712Kr.
Autosomal dominant

CHD8 overgrowth syndrome

ORPHA:642675Kr.
Autosomal dominant

CHILD syndrome

ORPHA:139Kr.
X-linked dominant

CHST3-related skeletal dysplasia

ORPHA:263463Kr.
Autosomal recessive