congenital dyserythropoietic anemia type Ib

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Summary

Literature (0)

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: CDAN1B, CDA, type Ib

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cdin1

MIM:

MIM:615631 - ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B

MIM:615631 - ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), congenital dyserythropoietic anemia type I (is_a)