D55.3
BillableAnemia due to disorders of nucleotide metabolism
Anemia due to disorders of nucleotide metabolism
Coding Notes
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) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(5)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(19)
SNOMED CT
- HNSHA due to pyrimidine-5'-nucleotidase deficiency34194007
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to pyrimidine-5'-nucleotidase deficiency34194007
- Hereditary nonspherocytic haemolytic anaemia due to pyrimidine-5'-nucleotidase deficiency34194007
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to pyrimidine-5'-nucleotidase deficiency34194007
- Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency34194007
- Anaemia due to disorders of nucleotide metabolism191180008
- Anemia due to disorders of nucleotide metabolism191180008
UMLS
Clinical Terms
- Anaemia due to disorders of nucleotide metabolism
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to pyrimidine-5'-nucleotidase deficiency
- HNSHA due to pyrimidine-5'-nucleotidase deficiency
- Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency
- Anemia due to Disorder of Nucleotide Metabolism
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to pyrimidine-5'-nucleotidase deficiency
- Hereditary nonspherocytic haemolytic anaemia due to pyrimidine-5'-nucleotidase deficiency
- Anemia due to disorders of nucleotide metabolism (disorder)
Frequently Asked Questions
What is the ICD-10 code for anemia due to disorders of nucleotide metabolism?
The ICD-10-CM code for anemia due to disorders of nucleotide metabolism is D55.3. The full clinical description is "Anemia due to disorders of nucleotide metabolism". D55.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D55.3 mean?
ICD-10-CM code D55.3 represents “Anemia due to disorders of nucleotide metabolism”. 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 D55.3 a billable code?
Yes, D55.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D55.3 in?
D55.3 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D55.3?
D55.3 has Excludes1 notes indicating codes that cannot be used together with it, including: drug-induced enzyme deficiency anemia (D59.2).
What SNOMED CT codes does D55.3 map to?
D55.3 maps to 2 SNOMED CT concepts: 191180008, 34194007. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D55.3?
D55.3 is linked to 1 UMLS Concept Unique Identifier: C0475533. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D55.3 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like anemia due to disorders of nucleotide metabolism 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 D55.3?
D55.3 maps to the ICD-11 code: 3A10.Z (Hereditary haemolytic anaemia, unspecified).
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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.