AutoICD API

D58.2

Billable

Other hemoglobinopathies

Other hemoglobinopathies

Status

Billable / Specific

Block

D55-D59

Parent Code

D58

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Abnormal hemoglobin NOS
  • Congenital Heinz body anemia
  • Hb-C disease
  • Hb-D disease
  • Hb-E disease
  • Hemoglobinopathy NOS
  • Unstable hemoglobin hemolytic disease

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

BillableD58.1

Hereditary elliptocytosis

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.ZHereditary haemolytic anaemia, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(437)

SNOMED CT

UMLS

Clinical Terms

  • hemoglobin e disease
  • Aseptic necrosis of bone due to hemoglobinopathy
  • Osteonecrosis of multiple sites due to hemoglobinopathy
  • Hemoglobin D disease (disorder)
  • Hemoglobin-C Disease
  • Homozygous hemoglobinopathy
  • Osteonecrosis of bone of forearm due to hemoglobinopathy
  • Abnormal Hb
  • Haemoglobin C trait
  • Osteonecrosis of pelvic region due to haemoglobinopathy
  • Acquired hemoglobinopathy
  • Hemoglobin E-E disease
  • Avascular necrosis of femur due to haemoglobinopathy
  • Hemoglobin C disease
  • Hemoglobin-C Diseases
  • Hb-E disease
  • Haemoglobin O-Arab trait
  • Hemoglobin C-A disorder
  • Unstable haemoglobin disease
  • Trait haemoglobinopathy
  • C Disease, Hemoglobin
  • Trait hemoglobinopathy
  • Aseptic necrosis of bone of forearm due to hemoglobinopathy
  • Acquired haemoglobinopathy
  • Avascular necrosis of bones of multiple regions due to haemoglobinopathy
  • Avascular necrosis of bone of ankle joint region due to hemoglobinopathy
  • Haemoglobin Iraq-Halabja trait
  • Hereditary haemoglobinopathy
  • Congenital Heinz body anemia
  • Avascular necrosis of bone of lower leg due to hemoglobinopathy
  • Avascular necrosis of bone of pelvic region due to haemoglobinopathy
  • Heterozygous for Hb D
  • Aseptic necrosis of femur due to haemoglobinopathy
  • Hemoglobin D Disease
  • Hemoglobin E disease (disorder)
  • Homozygous haemoglobinopathy
  • hemoglobin disease
  • Haemoglobin abnormal NOS
  • Aseptic necrosis of femur due to hemoglobinopathy
  • Hemoglobin C-C disease
  • Heterozygous for Hb C
  • Haemoglobinopathy NOS
  • Hemoglobin E-A disorder
  • haemoglobin disease
  • Avascular necrosis of femur due to hemoglobinopathy
  • Low affinity hemoglobin
  • Mixed hemoglobinopathy
  • Avascular necrosis of bone due to hemoglobinopathy
  • Low affinity haemoglobin
  • Unstable hemoglobin disease (disorder)
  • Osteonecrosis due to haemoglobinopathy
  • Hemoglobin C disease (disorder)
  • Osteonecrosis of lower leg due to haemoglobinopathy
  • Hemoglobin E trait
  • Haemoglobin disorder
  • CHBHA - Congenital Heinz body haemolytic anaemia
  • Osteonecrosis of ankle due to hemoglobinopathy
  • Osteonecrosis of multiple sites due to haemoglobinopathy
  • hemoglobin disorder
  • Haemoglobin D disease
  • Hemoglobin D-D disease
  • Hereditary hemoglobinopathy
  • Abnormal hemoglobin
  • Hb-C disease
  • disorders hemoglobin
  • Aseptic necrosis of humerus due to hemoglobinopathy
  • Haemoglobin C-A disorder
  • Homozygous for Hb C
  • Mixed haemoglobinopathy
  • Aseptic necrosis of bone of pelvic region due to hemoglobinopathy
  • Unstable hemoglobin hemolytic disease
  • Osteonecrosis of pelvic region due to hemoglobinopathy
  • Hereditary hemoglobinopathy due to globin chain mutation
  • Sickle Cell-Hemoglobin D Disease
  • PXE - Pseudoxanthoma elasticum
  • Haemoglobin E disease
  • Osteonecrosis of hand due to haemoglobinopathy
  • Osteonecrosis of humerus due to haemoglobinopathy
  • Haemoglobin E-A disorder
  • Haemoglobinopathies congenital
  • Heterozygous haemoglobinopathy
  • Osteonecrosis of pelvis
  • Haemoglobin D-A disorder
  • Pseudoxanthoma elasticum due to haemoglobinopathy
  • Hemoglobinopathies
  • Avascular necrosis of bone of foot due to hemoglobinopathy
  • Mixed hemoglobin disorder
  • Homozygous haemoglobin E
  • Avascular necrosis of bone of forearm due to haemoglobinopathy
  • C Diseases, Hemoglobin
  • Avascular necrosis of bones of multiple regions due to hemoglobinopathy
  • Pseudoxanthoma elasticum
  • Congenital Heinz body hemolytic anemia
  • Aseptic necrosis of lower leg due to hemoglobinopathy
  • CHBHA - Congenital Heinz body hemolytic anemia
  • Hemoglobin D-A disorder
  • Hemoglobin O-Arab trait
  • Aseptic necrosis of hand due to hemoglobinopathy
  • hemoglobin abnormal
  • Haemoglobin NOS abnormal
  • Haemoglobin C-C disease
  • Aseptic necrosis of bone of foot due to haemoglobinopathy
  • Hemoglobin Zurich disease
  • Haemoglobinopathy induced osteonecrosis
  • Aseptic necrosis of bone of ankle joint region due to haemoglobinopathy
  • Hemoglobin C trait
  • Hemoglobinopathy NOS
  • Hemoglobin C Diseases
  • Avascular necrosis of pelvis
  • Osteonecrosis of bone of forearm due to haemoglobinopathy
  • Structural haemoglobinopathy
  • Aseptic necrosis of bone due to haemoglobinopathy
  • Osteonecrosis due to hemoglobinopathy
  • Hemoglobinopathy (disorder)
  • Osteonecrosis of ankle due to haemoglobinopathy
  • Congenital Heinz body anaemia
  • High affinity haemoglobin
  • Transient neonatal cyanosis and anaemia due to Toms River Haemoglobin
  • haemoglobinopathies
  • Aseptic necrosis of lower leg due to haemoglobinopathy
  • Hemoglobin D trait
  • Pseudoxanthoma elasticum due to hemoglobinopathy
  • Aseptic necrosis of bone of forearm due to haemoglobinopathy
  • Avascular necrosis of bone of shoulder region due to haemoglobinopathy
  • Aseptic necrosis of humerus
  • Aseptic necrosis of pelvis
  • Osteonecrosis of femur due to haemoglobinopathy
  • Globin abnormality
  • Haemoglobinopathy Toms River
  • Osteonecrosis of humerus due to hemoglobinopathy
  • Haemoglobin D-D disease
  • Haemoglobin E trait
  • Haemoglobin C disease
  • Osteonecrosis of femur due to hemoglobinopathy
  • hemoglobin disorders
  • Osteonecrosis of foot due to hemoglobinopathy
  • Haemoglobin E-E disease
  • Unstable hemoglobin disease
  • Avascular necrosis of humerus
  • Acquired pseudoxanthoma elasticum
  • Aseptic necrosis of bone of shoulder region due to hemoglobinopathy
  • Avascular necrosis of bone of lower leg due to haemoglobinopathy
  • Aseptic necrosis of bones of multiple regions due to hemoglobinopathy
  • Aseptic necrosis of bone of pelvic region due to haemoglobinopathy
  • HEMOGLOBIN C DIS
  • Osteonecrosis of foot due to haemoglobinopathy
  • Osteonecrosis of humerus
  • Congenital Heinz body haemolytic anaemia
  • Hemoglobin Iraq-Halabja trait
  • Other haemoglobinopathies
  • Haemoglobin Zurich disease
  • Avascular necrosis of bone of pelvic region due to hemoglobinopathy
  • Avascular necrosis of bone of forearm due to hemoglobinopathy
  • Haemoglobinopathy
  • Hb-D disease
  • Hemoglobinopathies / Iron Metabolism
  • diseases e haemoglobin
  • Structural hemoglobinopathy
  • Haemoglobin D trait
  • Haemoglobinopathy with cyanosis
  • Homozygous for Hb E
  • Avascular necrosis of bone of shoulder region due to hemoglobinopathy
  • Osteonecrosis of lower leg due to hemoglobinopathy
  • Aseptic necrosis of bone of foot due to hemoglobinopathy
  • Homozygous hemoglobin E
  • Transient neonatal cyanosis and anemia due to Toms River Hemoglobin
  • Aseptic necrosis of humerus due to haemoglobinopathy
  • Avascular necrosis of humerus due to haemoglobinopathy
  • Haemoglobinopathy with erythrocytosis
  • Avascular necrosis of bone of ankle joint region due to haemoglobinopathy
  • Aseptic necrosis of hand due to haemoglobinopathy
  • hemoglobinopathy
  • High affinity hemoglobin
  • Hemoglobinopathy Toms River
  • Avascular necrosis of humerus due to hemoglobinopathy
  • Osteonecrosis of shoulder region due to haemoglobinopathy
  • Hemoglobinopathy induced osteonecrosis
  • Haemoglobin abnormal
  • Aseptic necrosis of bone of shoulder region due to haemoglobinopathy
  • Avascular necrosis of bone due to haemoglobinopathy
  • Osteonecrosis of hand due to hemoglobinopathy
  • Abnormal hemoglobin NOS
  • Heterozygous hemoglobinopathy
  • Heterozygous for Hb E
  • Aseptic necrosis of bones of multiple regions due to haemoglobinopathy
  • Avascular necrosis of bone of foot due to haemoglobinopathy
  • Hereditary haemoglobinopathy due to globin chain mutation
  • Abnormal haemoglobin
  • Aseptic necrosis of bone of ankle joint region due to hemoglobinopathy
  • diseases hemoglobin
  • Avascular necrosis of bone of hand due to haemoglobinopathy
  • Hemoglobinopathy with cyanosis
  • Hemoglobinopathy with erythrocytosis
  • Osteonecrosis of shoulder region due to hemoglobinopathy
  • Avascular necrosis of bone of hand due to hemoglobinopathy
  • Central cyanosis
  • Mixed haemoglobin disorder
Frequently Asked Questions
What is the ICD-10 code for other hemoglobinopathies?

The ICD-10-CM code for other hemoglobinopathies is D58.2. The full clinical description is "Other hemoglobinopathies". D58.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D58.2 mean?

ICD-10-CM code D58.2 represents “Other hemoglobinopathies”. 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 D58.2 a billable code?

Yes, D58.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D58.2 in?

D58.2 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D58.2?

D58.2 has Excludes1 notes indicating codes that cannot be used together with it, including: hemolytic anemia of the newborn (P55.-); familial polycythemia (D75.0); Hb-M disease (D74.0); and 5 more.

What SNOMED CT codes does D58.2 map to?

D58.2 maps to 39 SNOMED CT concepts: 127039000, 403401007, 203486002, 1162340005, 1162327000, and 34 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D58.2?

D58.2 is linked to 7 UMLS Concept Unique Identifiers: C0349705, C0019021, C0272006, C0019045, C0272080, and 2 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D58.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other hemoglobinopathies 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 D58.2?

D58.2 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.