D58.8
BillableOther specified hereditary hemolytic anemias
Other specified hereditary hemolytic anemias
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Stomatocytosis
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(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(77)
SNOMED CT
- Stomatocytosis3272007
- HPP - hereditary pyropoikilocytosis9434008
- Hereditary pyropoikilocytosis9434008
- Coombs negative haemolytic anaemia12189000
- Coombs negative hemolytic anemia12189000
- Hereditary hydrocytosis14087004
- Hereditary stomatocytosis14087004
- Rh deficiency syndrome37272000
- HNSHA due to decreased adenosine deaminase activity78908001
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to decreased adenosine deaminase activity78908001
- Hereditary nonspherocytic haemolytic anaemia due to decreased adenosine deaminase activity78908001
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to decreased adenosine deaminase activity78908001
- Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity78908001
- Dessicocytosis87994004
- Xerocytosis87994004
- Anaemia due to membrane defect111575000
- Anemia due to membrane defect111575000
- Congenital elliptocytosis191169008
- HE - hereditary elliptocytosis191169008
- Hereditary elliptocytosis191169008
- Hereditary ovalocytosis191169008
- Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism363041004
- Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism363041004
- Dehydrated hereditary stomatocytosis715526002
- Hereditary xerocytosis715526002
- Familial pseudohyperkalaemia717254007
- Familial pseudohyperkalemia717254007
- Overhydrated hereditary stomatocytosis722125003
- Familial haemolytic uraemic syndrome722721004
- Familial hemolytic uremic syndrome722721004
- Hereditary cryohydrocytosis with normal stomatin773489008
- CHC (hereditary cryohydrocytosis) type 2782911008
- Hereditary cryohydrocytosis type 2782911008
- Hereditary cryohydrocytosis with reduced stomatin782911008
- Stomatin-deficient cryohydrocytosis782911008
- sdCHC - stomatin-deficient cryohydrocytosis782911008
UMLS
Clinical Terms
- Anemia due to membrane defect
- Hereditary hydrocytosis
- Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity
- sdCHC - stomatin-deficient cryohydrocytosis
- Congenital elliptocytosis
- stomatocytosis
- Familial haemolytic uraemic syndrome
- Hereditary xerocytosis
- Dessicocytosis
- Hereditary stomatocytosis
- Dehydrated hereditary stomatocytosis
- Hereditary pyropoikilocytosis
- Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to decreased adenosine deaminase activity
- Hereditary ovalocytosis
- Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
- HNSHA due to decreased adenosine deaminase activity
- HE - hereditary elliptocytosis
- Coombs negative hemolytic anemia
- Hereditary cryohydrocytosis with normal stomatin
- Stomatocytosis (disorder)
- CHC (hereditary cryohydrocytosis) type 2
- Rh deficiency syndrome
- Stomatin-deficient cryohydrocytosis
- Hereditary cryohydrocytosis with reduced stomatin
- Hereditary nonspherocytic hemolytic anemia (HNSHA) due to decreased adenosine deaminase activity
- Hereditary cryohydrocytosis type 2
- HPP - hereditary pyropoikilocytosis
- Hereditary nonspherocytic haemolytic anaemia due to decreased adenosine deaminase activity
- Overhydrated hereditary stomatocytosis
- Anaemia due to membrane defect
- Xerocytosis
- Hereditary elliptocytosis
- Coombs negative haemolytic anaemia
- Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism
- Familial hemolytic uremic syndrome
- Familial pseudohyperkalemia
- Familial pseudohyperkalaemia
Frequently Asked Questions
What is the ICD-10 code for other specified hereditary hemolytic anemias?
The ICD-10-CM code for other specified hereditary hemolytic anemias is D58.8. The full clinical description is "Other specified hereditary hemolytic anemias". D58.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D58.8 mean?
ICD-10-CM code D58.8 represents “Other specified hereditary hemolytic anemias”. 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 D58.8 a billable code?
Yes, D58.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D58.8 in?
D58.8 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D58.8?
D58.8 has Excludes1 notes indicating codes that cannot be used together with it, including: hemolytic anemia of the newborn (P55.-).
What SNOMED CT codes does D58.8 map to?
D58.8 maps to 16 SNOMED CT concepts: 111575000, 782911008, 191169008, 363041004, 12189000, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D58.8?
D58.8 is linked to 2 UMLS Concept Unique Identifiers: C0154296, C0272048. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D58.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified hereditary hemolytic anemias 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 D58.8?
D58.8 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.