D58.9
BillableHereditary hemolytic anemia, unspecified
Hereditary hemolytic anemia, unspecified
Coding Notes
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(95)
SNOMED CT
- Hereditary haemolytic anaemia38911009
- Hereditary hemolytic anemia38911009
- Congenital haemolytic anaemia42601008
- Congenital hemolytic anemia42601008
- Megaloblastic anaemia due to chronic haemolytic anaemia47844003
- Megaloblastic anemia due to chronic hemolytic anemia47844003
- Haemolytic anaemia with emphysema AND cutis laxa60805002
- Hemolytic anemia with emphysema AND cutis laxa60805002
- Haemolytic anaemia61261009
- Hemolytic anemia61261009
- Associated pulmonary arterial hypertension697902002
- Pulmonary arterial hypertension associated with chronic haemolytic anaemia697908003
- Pulmonary arterial hypertension associated with chronic hemolytic anemia697908003
- Chronic haemolytic anaemia707480001
- Chronic hemolytic anemia707480001
- Lethal haemolytic anaemia and genital anomaly syndrome719402008
- Lethal hemolytic anemia and genital anomaly syndrome719402008
- Waters West syndrome719402008
UMLS
- ANEMIA HEMOLYTIC CONGENC0002881
- Anemia, Congenital HemolyticC0002881
- Anemia, Hemolytic, CongenitalC0002881
- Anemia, Hemolytic, HereditaryC0002881
- Anemia, Hereditary HemolyticC0002881
- Anemias, Congenital HemolyticC0002881
- Anemias, Hereditary HemolyticC0002881
- CONGEN HEMOLYTIC ANEMIAC0002881
- Congenital Hemolytic AnemiaC0002881
- Congenital Hemolytic AnemiasC0002881
- Congenital haemolytic anaemiaC0002881
- Congenital haemolytic anaemia NOSC0002881
- Congenital haemolytic anemiaC0002881
- Congenital hemolytic anaemiaC0002881
- Congenital hemolytic anemiaC0002881
- Congenital hemolytic anemia (disorder)C0002881
- HEMOLYTIC ANEMIA CONGENC0002881
- Hemolytic Anemia, CongenitalC0002881
- Hemolytic Anemia, HereditaryC0002881
- Hemolytic Anemias, CongenitalC0002881
- Hemolytic Anemias, HereditaryC0002881
- Hemolytic anemia, congenitalC0002881
- Hereditary Hemolytic AnemiaC0002881
- Hereditary Hemolytic AnemiasC0002881
- Hereditary haemolytic anaemiaC0002881
- Hereditary haemolytic anaemia NOSC0002881
- Hereditary haemolytic anaemia, unspecifiedC0002881
- Hereditary haemolytic anaemiasC0002881
- Hereditary hemolytic anemiaC0002881
- Hereditary hemolytic anemia (disorder)C0002881
- Hereditary hemolytic anemia, unspecifiedC0002881
- Hereditary hemolytic anemiasC0002881
- anaemias haemolytics hereditaryC0002881
- congenital hemolytic anemiaC0002881
- hereditary haemolytic anaemiasC0002881
- hereditary hemolytic anemiaC0002881
Clinical Terms
- Hemolytic anemia
- Congenital haemolytic anemia
- Hemolytic Anemia, Congenital
- Megaloblastic anemia due to chronic hemolytic anemia
- Congenital haemolytic anaemia
- Hemolytic Anemia, Hereditary
- Congenital Hemolytic Anemias
- Waters West syndrome
- Anemias, Congenital Hemolytic
- Associated pulmonary arterial hypertension
- Congenital Hemolytic Anemia
- Anemia, Congenital Hemolytic
- Anemia, Hereditary Hemolytic
- Congenital haemolytic anaemia NOS
- HEMOLYTIC ANEMIA CONGEN
- Hemolytic anemia with emphysema AND cutis laxa
- Pulmonary arterial hypertension associated with chronic haemolytic anaemia
- Hereditary haemolytic anaemia NOS
- Hemolytic Anemias, Hereditary
- Hereditary haemolytic anaemia, unspecified
- Anemia, Hemolytic, Congenital
- Hereditary haemolytic anaemia
- Anemias, Hereditary Hemolytic
- Lethal hemolytic anemia and genital anomaly syndrome
- Hereditary hemolytic anemia (disorder)
- ANEMIA HEMOLYTIC CONGEN
- Haemolytic anaemia with emphysema AND cutis laxa
- Congenital hemolytic anaemia
- Megaloblastic anaemia due to chronic haemolytic anaemia
- Congenital hemolytic anemia (disorder)
- hereditary haemolytic anaemias
- anaemias haemolytics hereditary
- Hereditary hemolytic anemias
- Haemolytic anaemia
- Anemia, Hemolytic, Hereditary
- CONGEN HEMOLYTIC ANEMIA
- Pulmonary arterial hypertension associated with chronic hemolytic anemia
- Chronic hemolytic anemia
- Lethal haemolytic anaemia and genital anomaly syndrome
- Hemolytic Anemias, Congenital
- Chronic haemolytic anaemia
Frequently Asked Questions
What is the ICD-10 code for hereditary hemolytic anemia, unspecified?
The ICD-10-CM code for hereditary hemolytic anemia, unspecified is D58.9. The full clinical description is "Hereditary hemolytic anemia, unspecified". D58.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D58.9 mean?
ICD-10-CM code D58.9 represents “Hereditary hemolytic anemia, unspecified”. 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 D58.9 a billable code?
Yes, D58.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D58.9 in?
D58.9 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D58.9?
D58.9 has Excludes1 notes indicating codes that cannot be used together with it, including: hemolytic anemia of the newborn (P55.-).
What SNOMED CT codes does D58.9 map to?
D58.9 maps to 9 SNOMED CT concepts: 697902002, 707480001, 42601008, 61261009, 60805002, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D58.9?
D58.9 is linked to 1 UMLS Concept Unique Identifier: C0002881. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D58.9 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary hemolytic anemia, unspecified 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 D58.9?
D58.9 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.