Familial hypohaptoglobinemia. A genetically determined trait segragating from glucose-6-phosphate dehydrogenase deficiency.
D001796:Blood Protein Disorders; D005954:Glucosephosphate Dehydrogenase; D005955:Glucosephosphate Dehydrogenase Deficiency; D006242:Haptoglobins; D006801:Humans; D010641:Phenotype
D006242:Haptoglobins; D005954:Glucosephosphate Dehydrogenase
BLOOD PROTEIN DISORDERS; GLUCOSEPHOSPHATE DEHYDROGENASE; HAPTOGLOBINS