ZFIN Human Disease: congenital dyserythropoietic anemia type Ia

OBO ID: DOID:0111398

Term Name:	congenital dyserythropoietic anemia type Ia		Search Ontology:
Synonyms:	CDA Ia CDAN1A
Definition:	A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in the CDAN1 gene on chromosome 15q15.2. https://www.ncbi.nlm.nih.gov/pubmed/12434312
References:	OMIM:224120
Ontology:	Human Disease ( DOID:0111398 )

Relationships

is a type of:	autosomal recessive disease congenital dyserythropoietic anemia type I autosomal recessive disease congenital dyserythropoietic anemia type I Show first 5 Terms

OTHER congenital dyserythropoietic anemia type Ia PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CDAN1	cdan1	Dyserythropoietic anemia, congenital, type Ia	224120

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None