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Metadata
ID	DOID:0051006
Name	congenital nonspherocytic hemolytic anemia 5
Definition	A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the HK1 gene, which encodes a form of hexokinase, on chromosome 10q22. https://pubmed.ncbi.nlm.nih.gov/12393545/
Xrefs	MIM:235700
Parent Relationships	is_a congenital nonspherocytic hemolytic anemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance