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Echinobase
Summary Literature (0)
DOID:0110920 - hereditary spherocytosis type 5

Disease Ontology Definition:A hereditary spherocytosis that has_material_basis_in a mutation of EPB42 on chromosome 15q15.2.

Synonyms: HS5, SPH5, hereditary spherocytosis 5,

Echinobase Genes :


OMIM:
MIM:612690 - spherocytosis, type 5; sph5

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary spherocytosis (is_a)