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Summary Literature (0)
DOID:0110919 - hereditary spherocytosis type 4


Disease Ontology Definition:A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SLC4A1 on chromosome 17q21.31.

Synonyms: HS4, SPH4, hereditary spherocytosis 4

In OMIM:
OMIM:612653 - SPHEROCYTOSIS, TYPE 4; SPH4

In Mondo Disease Ontology:
MONDO:0012981 - hereditary spherocytosis type 4

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : slc4a1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hereditary spherocytosis (is_a)