Term Name: congenital nonspherocytic hemolytic anemia 4
Synonyms:
Definition: A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHI gene (GPI) on chromosome 19q13.
Ontology: Human Disease [DOID:0051005]   ( DOID:0051005 )

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