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DOID:0110918 - hereditary spherocytosis type 3
Disease Ontology Definition:A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1.
Synonyms: HS3, SPH3, hereditary spherocytosis 3,
Xenbase Genes :
MONDO:0010053 - hereditary spherocytosis type 3 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee