Term Name: congenital nonspherocytic hemolytic anemia 5
Synonyms:
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.
Ontology: Human Disease [DOID:0051006]   ( DOID:0051006 )

Relationships
is a type of: autosomal recessive disease congenital nonspherocytic hemolytic anemia