AutoICD API

D58.1

Billable

Hereditary elliptocytosis

Hereditary elliptocytosis

Status

Billable / Specific

Block

D55-D59

Parent Code

D58

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Elliptocytosis (congenital)
  • Ovalocytosis (congenital) (hereditary)

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

Related Codes(4)
D58.0

Hereditary spherocytosis

BillableD58.2

Other hemoglobinopathies

BillableD58.8

Other specified hereditary hemolytic anemias

BillableD58.9

Hereditary hemolytic anemia, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

3A10.2Hereditary elliptocytosisequivalentPrimary
Also Known As / Clinical Terms(75)

SNOMED CT

UMLS

Clinical Terms

  • Elliptocytosis (congenital)
  • Homozygous hereditary elliptocytosis
  • Hereditary elliptocytosis with transient poikilocytosis
  • Hereditary Elliptocytoses
  • Congenital elliptocytosis
  • Elliptocytosis
  • Hereditary elliptocytosis due to alpha spectrin defect
  • Stomatocytic elliptocytosis
  • hereditary ovalocytosis
  • Melanesian ovalocytosis
  • Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
  • Hereditary Ovalocytoses
  • Hereditary elliptocytosis due to deficiency of protein 4.1
  • Hereditary elliptocytosis due to beta spectrin defect in self-association
  • ovalocytosis
  • Hereditary elliptocytosis (disorder)
  • AMME syndrome
  • elliptocytosis hereditary
  • Ovalocytosis, Hereditary
  • Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
  • Ovalocytoses, Hereditary
  • Stomatocytosis
  • HE - hereditary elliptocytosis
  • Hereditary elliptocytosis due to abnormal protein 4.1
  • Elliptocytoses, Hereditary
  • Hereditary elliptocytosis due to glycophorin C deficiency
  • Congenital nephritis
  • AMME complex
  • Ovalocytosis (congenital) (hereditary)
  • Southeast Asian ovalocytosis
  • Elliptocytosis, Hereditary
Frequently Asked Questions
What is the ICD-10 code for hereditary elliptocytosis?

The ICD-10-CM code for hereditary elliptocytosis is D58.1. The full clinical description is "Hereditary elliptocytosis". D58.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D58.1 mean?

ICD-10-CM code D58.1 represents “Hereditary elliptocytosis”. 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 D58.1 a billable code?

Yes, D58.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D58.1 in?

D58.1 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D58.1?

D58.1 has Excludes1 notes indicating codes that cannot be used together with it, including: hemolytic anemia of the newborn (P55.-).

What SNOMED CT codes does D58.1 map to?

D58.1 maps to 14 SNOMED CT concepts: 720982007, 191169008, 276585000, 250242004, 75443009, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D58.1?

D58.1 is linked to 1 UMLS Concept Unique Identifier: C0013902. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D58.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary elliptocytosis 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 D58.1?

D58.1 maps to the ICD-11 code: 3A10.2 (Hereditary elliptocytosis).

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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.