D55.29

Billable

Anemia due to other disorders of glycolytic enzymes

Anemia due to other disorders of glycolytic enzymes

Status

Billable / Specific

Block

D55-D59

Parent Code

D55.2

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Hexokinase deficiency anemia
  • Triose-phosphate isomerase 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

Related Codes(1)
D55.21

Anemia due to pyruvate kinase deficiency

Billable
Also Known As / Clinical Terms(96)

SNOMED CT

UMLS

Clinical Terms

  • Hexokinase deficiency anaemia
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to glucose phosphate isomerase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency
  • HNSHA due to NADH diaphorase deficiency
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency
  • Haemolytic anaemia due to red cell enolase deficiency
  • HNSHA due to phosphoglycerate kinase deficiency
  • Hemolytic anemia due to hexokinase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to triosephosphate isomerase deficiency
  • Haemolytic anaemia due to triose phosphate isomerase deficiency
  • Haemolytic anaemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
  • HNSHA due to triosephosphate isomerase deficiency
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphofructokinase deficiency
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to triosephosphate isomerase deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to phosphoglycerate kinase deficiency
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency
  • Hexokinase deficiency anemia
  • Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder)
  • Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency
  • HNSHA due to hexokinase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to phosphofructokinase deficiency
  • Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphoglycerate kinase deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to triosephosphate isomerase deficiency
  • HNSHA due to glucose phosphate isomerase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to glucose phosphate isomerase deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to phosphofructokinase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to glucose phosphate isomerase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency
  • Haemolytic anaemia due to hexokinase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to phosphoglycerate kinase deficiency
  • Hemolytic anemia due to red cell enolase deficiency
  • Triosephosphate deficiency anaemia
  • Triosephosphate deficiency anemia
  • Triose-phosphate isomerase deficiency anemia
  • HNSHA due to phosphofructokinase deficiency
  • Hemolytic anemia due to triose phosphate isomerase deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency
Frequently Asked Questions
What is the ICD-10 code for anemia due to other disorders of glycolytic enzymes?

The ICD-10-CM code for anemia due to other disorders of glycolytic enzymes is D55.29. The full clinical description is "Anemia due to other disorders of glycolytic enzymes". D55.29 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D55.29 mean?

ICD-10-CM code D55.29 represents “Anemia due to other disorders of glycolytic enzymes”. 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 D55.29 a billable code?

Yes, D55.29 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D55.29 in?

D55.29 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D55.29?

D55.29 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 D55.29 map to?

D55.29 maps to 10 SNOMED CT concepts: 47526003, 52413004, 42484009, 41387000, 59644002, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D55.29?

D55.29 is linked to 3 UMLS Concept Unique Identifiers: C5539136, C0272063, C1387506. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D55.29 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like anemia due to other disorders of glycolytic enzymes affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of D55.29?

There is no direct ICD-11 mapping available for D55.29 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.