Term Name: congenital nonspherocytic hemolytic anemia 8
Synonyms:
Definition: A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the UMPH1 gene (NT5C3A) on chromosome 7p14.
Ontology: Human Disease [DOID:0051007]   ( DOID:0051007 )

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