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DOID:0110919 - hereditary spherocytosis type 4
Disease Ontology Definition:A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SLC4A1 gene on chromosome 17q21.31.
Synonyms: HS4, SPH4, hereditary spherocytosis 4,
Echinobase Genes :
MIM:612653 - spherocytosis, type 4; sph4 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee