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DOID:0110920 - hereditary spherocytosis type 5
Disease Ontology Definition:A hereditary spherocytosis that has_material_basis_in a mutation of the EPB42 gene on chromosome 15q15.2.
Synonyms: HS5, SPH5, hereditary spherocytosis 5,
Xenbase Genes : epb42
MONDO:0012985 - hereditary spherocytosis type 5 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee