D55.29
BillableAnemia due to other disorders of glycolytic enzymes
Anemia due to other disorders of glycolytic enzymes
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
- 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 due to phosphofructokinase deficiency41387000
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to phosphofructokinase deficiency41387000
- Hereditary nonspherocytic haemolytic anaemia due to phosphofructokinase deficiency41387000
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphofructokinase deficiency41387000
- Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency41387000
- HNSHA due to hexokinase deficiency42484009
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiency42484009
- Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiency42484009
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency42484009
- Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency42484009
- Hexokinase deficiency anaemia42484009
- Hexokinase deficiency anemia42484009
- HNSHA due to triosephosphate isomerase deficiency44641000
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to triosephosphate isomerase deficiency44641000
- Hereditary nonspherocytic haemolytic anaemia due to triosephosphate isomerase deficiency44641000
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to triosephosphate isomerase deficiency44641000
- Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency44641000
- Triosephosphate deficiency anaemia44641000
- Triosephosphate deficiency anemia44641000
- HNSHA due to NADH diaphorase deficiency47526003
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency47526003
- Hereditary nonspherocytic haemolytic anaemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency47526003
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency47526003
- Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency47526003
- HNSHA due to glucose phosphate isomerase deficiency52413004
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to glucose phosphate isomerase deficiency52413004
- Hereditary nonspherocytic haemolytic anaemia due to glucose phosphate isomerase deficiency52413004
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to glucose phosphate isomerase deficiency52413004
- Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency52413004
- HNSHA due to phosphoglycerate kinase deficiency59644002
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to phosphoglycerate kinase deficiency59644002
- Hereditary nonspherocytic haemolytic anaemia due to phosphoglycerate kinase deficiency59644002
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphoglycerate kinase deficiency59644002
- Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency59644002
- Haemolytic anaemia due to hexokinase deficiency191177007
- Hemolytic anemia due to hexokinase deficiency191177007
- Haemolytic anaemia due to triose phosphate isomerase deficiency191179005
- Hemolytic anemia due to triose phosphate isomerase deficiency191179005
- Haemolytic anaemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency1148893001
- Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency1148893001
- Haemolytic anaemia due to red cell enolase deficiency1148895008
- Hemolytic anemia due to red cell enolase deficiency1148895008
UMLS
- Anemia due to other disorders of glycolytic enzymesC5539136
- HNSHA due to hexokinase deficiencyC0272063
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiencyC0272063
- Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiencyC0272063
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiencyC0272063
- Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiencyC0272063
- Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder)C0272063
- Hexokinase deficiency anaemiaC0272063
- Hexokinase deficiency anemiaC0272063
- Triose-phosphate isomerase deficiency anemiaC1387506
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.
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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.