ICD 10 CM Codes

D55.2 Anemia due to disorders of glycolytic enzymes
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM D55.2 converts approximately to:ICD-9-CM
2015 ICD-9-CM 282.3 Other hemolytic anemias due to enzyme deficiency
ICD-10-CM D55.2is grouped within Diagnostic Related Group(s) (MS-DRG v30.0)
811 RED BLOOD CELL DISORDERS WITH MCC
812 RED BLOOD CELL DISORDERS WITHOUT MCC
Type 1 Excludes
disorders of glycolysis not associated with anemia (E74.8)
Alternate Description
Hemolytic nonspherocytic (hereditary) anemia, type II
Hexokinase deficiency anemia
Pyruvate kinase [PK] deficiency anemia
Triose-phosphate isomerase deficiency anemia
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.D55.2.'
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); with (due to) (in); disorder of; anaerobic glycolysis
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; 2, 3 diphosphoglycurate mutase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; 2, 3 PG
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; enzyme; glycolytic
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; glyceraldehyde phosphate dehydrogenase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; hexokinase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; phosphofructo-aldolase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; phosphoglycerate kinase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; PK
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; pyruvate kinase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); deficiency; triose-phosphate isomerase
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); hemolytic; nonspherocytic; congenital or hereditary NEC; pyruvate kinase deficiency
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); hemolytic; nonspherocytic; congenital or hereditary NEC; type; II
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); hemolytic; nonspherocytic; type; II
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); hexokinase deficiency
Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound); pyruvate kinase deficiency
Disorder (of); anaerobic glycolysis with anemia