MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Cystic fibrosis

ORPHA:586Disease
Autosomal recessive

Cystic fibrosis-gastritis-megaloblastic anemia syndrome

ORPHA:2575Disease
Autosomal recessive

Cystic hamartoma of lung and kidney

ORPHA:2111Disease
Unknown

Cystic leukoencephalopathy without megalencephaly

ORPHA:85136Disease
Autosomal recessive

Cysticercosis

ORPHA:1560Disease
Not applicable

Cystinosis

ORPHA:213Disease
Autosomal recessive

Cystinuria

ORPHA:214Disease
Autosomal recessive, Semi-dominant

Cystoid macular dystrophy

ORPHA:75381Disease
Autosomal dominant

Cytophagic histiocytic panniculitis

ORPHA:94087Disease
Unknown

Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder

ORPHA:477787Disease
Autosomal recessive

D,L-2-hydroxyglutaric aciduria

ORPHA:356978Disease
Autosomal recessive

D-2-hydroxyglutaric aciduria

ORPHA:79315Disease
Autosomal dominant, Autosomal recessive

D-glyceric aciduria

ORPHA:941Disease
Autosomal recessive

DDOST-CDG

ORPHA:300536Disease
Autosomal recessive

DDX41-related hematologic malignancy predisposition syndrome

ORPHA:488647Disease
Multigenic/multifactorial

DEND syndrome

ORPHA:79134Disease
Autosomal dominant, Autosomal recessive, Not applicable

DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome

ORPHA:494444Disease
Autosomal dominant

DICER1 tumor-predisposition syndrome

ORPHA:284343Disease
Autosomal dominant

DITRA

ORPHA:404546Disease
Autosomal recessive

DK1-CDG

ORPHA:91131Disease
Autosomal recessive

DNA2-related mitochondrial DNA deletion syndrome

ORPHA:352470Disease
Autosomal dominant

DNAJB2-related Charcot-Marie-Tooth disease type 2

ORPHA:443950Disease
Autosomal recessive

DNAJB4-related distal myopathy

ORPHA:700170Disease
Autosomal dominant

DNAJB6-related distal myopathy

ORPHA:708126Disease
Autosomal dominant