D55.21
BillableAnemia due to pyruvate kinase deficiency
Anemia due to pyruvate kinase deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- PK deficiency anemia
- Pyruvate kinase deficiency anemia
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency74703006
- HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency74703006
- Hereditary nonspherocytic haemolytic anaemia due to pyruvate kinase deficiency74703006
- Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency74703006
- PK (pyruvate kinase) deficiency haemolytic anaemia74703006
- PK (pyruvate kinase) deficiency hemolytic anemia74703006
- Pyruvate kinase deficiency anaemia74703006
- Pyruvate kinase deficiency anemia74703006
UMLS
- Anemia due to pyruvate kinase deficiencyC5539135
- HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiencyC0272062
- HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiencyC0272062
- Hereditary nonspherocytic haemolytic anaemia due to pyruvate kinase deficiencyC0272062
- Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiencyC0272062
- Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (disorder)C0272062
- PK (pyruvate kinase) deficiency haemolytic anaemiaC0272062
- PK (pyruvate kinase) deficiency hemolytic anemiaC0272062
- PK deficiency anemiaC0272062
- Pyruvate kinase deficiency anaemiaC0272062
- Pyruvate kinase deficiency anemiaC0272062
Frequently Asked Questions
What is the ICD-10 code for anemia due to pyruvate kinase deficiency?
The ICD-10-CM code for anemia due to pyruvate kinase deficiency is D55.21. The full clinical description is "Anemia due to pyruvate kinase deficiency". D55.21 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D55.21 mean?
ICD-10-CM code D55.21 represents "Anemia due to pyruvate kinase deficiency". It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D55.21 a billable code?
Yes, D55.21 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D55.21 in?
D55.21 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D55.21?
D55.21 has Excludes1 notes indicating codes that cannot be used together with it, including: drug-induced enzyme deficiency anemia (D59.2); disorders of glycolysis not associated with anemia (E74.81-).
What SNOMED CT codes does D55.21 map to?
D55.21 maps to 1 SNOMED CT concept: 74703006. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D55.21?
D55.21 is linked to 2 UMLS Concept Unique Identifiers: C5539135, C0272062. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.