Cytoscape Web
Click node...

Congenital dyserythropoietic anemia type I
2 OMIM references -
2 associated genes
1 connected disease
No signs/symptoms info
Disease Type of connection
Autosomal dominant macrothrombocytopenia
Synonym(s):
- CDA I
- CDA type 1
- CDA type I
- Congenital dyserythropoietic anemia type 1
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: adult
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
C15ORF41 Q9Y2V0615626
CDAN1 Q8IWY9607465
No signs/symptoms info available.