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)
- hemolytic anemia of the newborn (P55.-)
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
- 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
Frequently Asked Questions
What is ICD-10 code D58.8?
ICD-10-CM code D58.8 represents "Other specified hereditary hemolytic anemias". It 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.
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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.