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DO Term : congenital dyserythropoietic anemia type Ia [DOID:0111398] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in the CDAN1 gene on chromosome 15q15.2.

synonyms:
OMIM:224120,
CDAN1A,
CDA Ia,
224120

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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