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Metadata
ID	DOID:0051005
Name	congenital nonspherocytic hemolytic anemia 4
Definition	A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHI gene (GPI) on chromosome 19q13. https://pubmed.ncbi.nlm.nih.gov/8218542/
Xrefs	MIM:613470
Parent Relationships	is_a congenital nonspherocytic hemolytic anemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance