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

Cystic fibrosis

ORPHA:586Kr.
Autosomal recessive

Cystic fibrosis-gastritis-megaloblastic anemia syndrome

ORPHA:2575Kr.
Autosomal recessive

Cystic hamartoma of lung and kidney

ORPHA:2111Kr.
Unknown

Cystic leukoencephalopathy without megalencephaly

ORPHA:85136Kr.
Autosomal recessive

Cysticercosis

ORPHA:1560Kr.
Not applicable

Cystinosis

ORPHA:213Kr.
Autosomal recessive

Cystinuria

ORPHA:214Kr.
Autosomal recessive, Semi-dominant

Cystoid macular dystrophy

ORPHA:75381Kr.
Autosomal dominant

Cytophagic histiocytic panniculitis

ORPHA:94087Kr.
Unknown

Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder

ORPHA:477787Kr.
Autosomal recessive

D,L-2-hydroxyglutaric aciduria

ORPHA:356978Kr.
Autosomal recessive

D-2-hydroxyglutaric aciduria

ORPHA:79315Kr.
Autosomal dominant, Autosomal recessive

D-glyceric aciduria

ORPHA:941Kr.
Autosomal recessive

DDOST-CDG

ORPHA:300536Kr.
Autosomal recessive

DDX41-related hematologic malignancy predisposition syndrome

ORPHA:488647Kr.
Multigenic/multifactorial

DEND syndrome

ORPHA:79134Kr.
Autosomal dominant, Autosomal recessive, Not applicable

DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome

ORPHA:494444Kr.
Autosomal dominant

DICER1 tumor-predisposition syndrome

ORPHA:284343Kr.
Autosomal dominant

DITRA

ORPHA:404546Kr.
Autosomal recessive

DK1-CDG

ORPHA:91131Kr.
Autosomal recessive

DNA2-related mitochondrial DNA deletion syndrome

ORPHA:352470Kr.
Autosomal dominant

DNAJB2-related Charcot-Marie-Tooth disease type 2

ORPHA:443950Kr.
Autosomal recessive

DNAJB4-related distal myopathy

ORPHA:700170Kr.
Autosomal dominant

DNAJB6-related distal myopathy

ORPHA:708126Kr.
Autosomal dominant