|
DOID:0111397 - congenital dyserythropoietic anemia type Ib
Disease Ontology Definition:A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in C15orf41 on chromosome 15q14.
Synonyms: CDA, type Ib, CDAN1B,
Xenbase Genes : cdin1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee