ICD 10 CM Codes

D55.1 Anemia due to other disorders of glutathione metabolism
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
ICD-10-CM D55.1 converts approximately to:ICD-9-CM
2018 ICD-9-CM 282.2 Anemias due to disorders of glutathione metabolism
Alternate Description
Anemia (due to) enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway
Anemia (due to) hemolytic nonspherocytic (hereditary), type I
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.D55.1.'
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); with (due to) (in); disorder of; pentose phosphate pathway
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; 6 phosphogluconate dehydrogenase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; 6-PGD
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; enzyme; related to hexose monophosphate (HMP) shunt pathway NEC
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; erythrocytic glutathione
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; G SH
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; GGS-R
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; glutathione reductase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); due to (in) (with); disorder of; glutathione metabolism
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); erythrocytic glutathione deficiency
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); glutathione-reductase deficiency
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); hemolytic; nonspherocytic; congenital or hereditary NEC; type; I
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); hemolytic; nonspherocytic; type; I
Disorder (of); pentose phosphate pathway with anemia