X-linked congenital hemolytic anemia

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Summary

Literature (0)

DOID:0111846 - X-linked congenital hemolytic anemia

Disease Ontology Definition:A congenital hemolytic anemia characterized by mild congenital hemolytic anemia without morphologic red cell abnormalities that has_material_basis_in hemizygous mutation in the ATP11C gene on chromosome Xq27.1.

Synonyms:

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

: atp11c

MIM:

MIM:301015 - HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED; HACXL

MIM:301015 - HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED; HACXL

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

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

Parent(s): congenital hemolytic anemia (is_a), X-linked recessive disease (is_a)