D58.0
BillableHereditary spherocytosis
Hereditary spherocytosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Acholuric (familial) jaundice
- Congenital (spherocytic) hemolytic icterus
- Minkowski-Chauffard syndrome
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
- Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin10564005
- Spherocytosis17235000
- Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin24975009
- Hereditary spherocytosis due to spectrin deficiency25266006
- Mild hereditary spherocytosis due to spectrin deficiency32648007
- Hereditary spherocytosis due to deficiency of protein 4.233905008
- Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin47516005
- Congenital spherocytic haemolytic anaemia55995005
- Congenital spherocytic hemolytic anemia55995005
- Congenital spherocytosis55995005
- Familial acholuric jaundice55995005
- Familial spherocytosis55995005
- HS - Hereditary spherocytosis55995005
- Hereditary spherocytosis55995005
- Minkowsky-Chauffard syndrome55995005
- Hereditary spherocytosis due to beta spectrin defect69981004
- Severe hereditary spherocytosis due to spectrin deficiency77413008
UMLS
- Acholuric (familial) jaundiceC0037889
- Anaemia spherocyticC0037889
- Anemia spherocyticC0037889
- Congenital spherocytic haemolytic anaemiaC0037889
- Congenital spherocytic hemolytic anemiaC0037889
- Congenital spherocytosisC0037889
- Familial acholuric jaundiceC0037889
- Familial spherocytosisC0037889
- HS - Hereditary spherocytosisC0037889
- Hereditary SpherocytosesC0037889
- Hereditary SpherocytosisC0037889
- Hereditary spherocytosisC0037889
- Hereditary spherocytosis (disorder)C0037889
- Minkowski Chauffard syndromeC0037889
- Minkowski-Chauffard syndromeC0037889
- Minkowsky-Chauffard syndromeC0037889
- Spherocytic anaemiaC0037889
- Spherocytic anemiaC0037889
- Spherocytoses, HereditaryC0037889
- Spherocytosis, HereditaryC0037889
- congenital spherocytosisC0037889
- familial spherocytosisC0037889
- hereditary spherocytosisC0037889
- spherocytic anemiaC0037889
- spherocytic hemolytic anemiaC0037889
- spherocytosis hereditaryC0037889
- Congenital (spherocytic) hemolytic icterusC2873774
Frequently Asked Questions
What is ICD-10 code D58.0?
ICD-10-CM code D58.0 represents "Hereditary spherocytosis". It is a billable/specific code that can be used on a claim.
Is D58.0 a billable code?
Yes, D58.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D58.0 in?
D58.0 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D58.0?
D58.0 has Excludes1 notes indicating codes that cannot be used together with it, including: hemolytic anemia of the newborn (P55.-).
What SNOMED CT codes does D58.0 map to?
D58.0 maps to 10 SNOMED CT concepts: 55995005, 69981004, 47516005, 33905008, 25266006, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D58.0?
D58.0 is linked to 2 UMLS Concept Unique Identifiers: C0037889, C2873774. 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.