D58.2
BillableOther hemoglobinopathies
Other hemoglobinopathies
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
- 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
- Haemoglobin D trait7391009
- Haemoglobin D-A disorder7391009
- Hemoglobin D trait7391009
- Hemoglobin D-A disorder7391009
- Heterozygous for Hb D7391009
- CHBHA - Congenital Heinz body haemolytic anaemia18273004
- CHBHA - Congenital Heinz body hemolytic anemia18273004
- Congenital Heinz body anaemia18273004
- Congenital Heinz body anemia18273004
- Congenital Heinz body haemolytic anaemia18273004
- Congenital Heinz body hemolytic anemia18273004
- Unstable haemoglobin disease18273004
- Unstable hemoglobin disease18273004
- Haemoglobin E disease25065001
- Haemoglobin E-E disease25065001
- Hemoglobin E disease25065001
- Hemoglobin E-E disease25065001
- Homozygous for Hb E25065001
- Mixed haemoglobin disorder38589006
- Mixed haemoglobinopathy38589006
- Mixed hemoglobin disorder38589006
- Mixed hemoglobinopathy38589006
- Haemoglobin E trait46248003
- Haemoglobin E-A disorder46248003
- Hemoglobin E trait46248003
- Hemoglobin E-A disorder46248003
- Heterozygous for Hb E46248003
- Haemoglobin C disease51053007
- Haemoglobin C-C disease51053007
- Hemoglobin C disease51053007
- Hemoglobin C-C disease51053007
- Homozygous for Hb C51053007
- Haemoglobin D disease66729008
- Haemoglobin D-D disease66729008
- Hemoglobin D disease66729008
- Hemoglobin D-D disease66729008
- Haemoglobinopathy with erythrocytosis75063005
- Hemoglobinopathy with erythrocytosis75063005
- Haemoglobin C trait76050008
- Haemoglobin C-A disorder76050008
- Hemoglobin C trait76050008
- Hemoglobin C-A disorder76050008
- Heterozygous for Hb C76050008
- Globin abnormality80141007
- Haemoglobin disease80141007
- Haemoglobin disorder80141007
- Haemoglobinopathy80141007
- Hemoglobin disease80141007
- Hemoglobin disorder80141007
- Hemoglobinopathy80141007
- Haemoglobinopathy with cyanosis84260001
- Hemoglobinopathy with cyanosis84260001
- Central cyanosis95837007
- Homozygous haemoglobinopathy123772008
- Homozygous hemoglobinopathy123772008
- Heterozygous haemoglobinopathy123773003
- Heterozygous hemoglobinopathy123773003
- Trait haemoglobinopathy123773003
- Trait hemoglobinopathy123773003
- Hereditary haemoglobinopathy due to globin chain mutation127038008
- Hereditary hemoglobinopathy due to globin chain mutation127038008
- Structural haemoglobinopathy127038008
- Structural hemoglobinopathy127038008
- Acquired haemoglobinopathy127039000
- Acquired hemoglobinopathy127039000
- Haemoglobin Zurich disease191202009
- Hemoglobin Zurich disease191202009
- Aseptic necrosis of bone due to haemoglobinopathy203486002
- Aseptic necrosis of bone due to hemoglobinopathy203486002
- Avascular necrosis of bone due to haemoglobinopathy203486002
- Avascular necrosis of bone due to hemoglobinopathy203486002
- Haemoglobinopathy induced osteonecrosis203486002
- Hemoglobinopathy induced osteonecrosis203486002
- Osteonecrosis due to haemoglobinopathy203486002
- Osteonecrosis due to hemoglobinopathy203486002
- Low affinity haemoglobin234393007
- Low affinity hemoglobin234393007
- High affinity haemoglobin234394001
- High affinity hemoglobin234394001
- PXE - Pseudoxanthoma elasticum252246005
- Pseudoxanthoma elasticum252246005
- Acquired pseudoxanthoma elasticum403401007
- Hereditary haemoglobinopathy427306008
- Hereditary hemoglobinopathy427306008
- Haemoglobin O-Arab trait445542007
- Hemoglobin O-Arab trait445542007
- Haemoglobinopathy Toms River782880001
- Hemoglobinopathy Toms River782880001
- Transient neonatal cyanosis and anaemia due to Toms River Haemoglobin782880001
- Transient neonatal cyanosis and anemia due to Toms River Hemoglobin782880001
- Aseptic necrosis of lower leg due to haemoglobinopathy1162321004
- Aseptic necrosis of lower leg due to hemoglobinopathy1162321004
- Avascular necrosis of bone of lower leg due to haemoglobinopathy1162321004
- Avascular necrosis of bone of lower leg due to hemoglobinopathy1162321004
- Osteonecrosis of lower leg due to haemoglobinopathy1162321004
- Osteonecrosis of lower leg due to hemoglobinopathy1162321004
- Aseptic necrosis of bones of multiple regions due to haemoglobinopathy1162324007
- Aseptic necrosis of bones of multiple regions due to hemoglobinopathy1162324007
- Avascular necrosis of bones of multiple regions due to haemoglobinopathy1162324007
- Avascular necrosis of bones of multiple regions due to hemoglobinopathy1162324007
- Osteonecrosis of multiple sites due to haemoglobinopathy1162324007
- Osteonecrosis of multiple sites due to hemoglobinopathy1162324007
- Aseptic necrosis of hand due to haemoglobinopathy1162325008
- Aseptic necrosis of hand due to hemoglobinopathy1162325008
- Avascular necrosis of bone of hand due to haemoglobinopathy1162325008
- Avascular necrosis of bone of hand due to hemoglobinopathy1162325008
- Osteonecrosis of hand due to haemoglobinopathy1162325008
- Osteonecrosis of hand due to hemoglobinopathy1162325008
- Aseptic necrosis of humerus due to haemoglobinopathy1162326009
- Aseptic necrosis of humerus due to hemoglobinopathy1162326009
- Avascular necrosis of humerus due to haemoglobinopathy1162326009
- Avascular necrosis of humerus due to hemoglobinopathy1162326009
- Osteonecrosis of humerus due to haemoglobinopathy1162326009
- Osteonecrosis of humerus due to hemoglobinopathy1162326009
- Aseptic necrosis of bone of foot due to haemoglobinopathy1162327000
- Aseptic necrosis of bone of foot due to hemoglobinopathy1162327000
- Avascular necrosis of bone of foot due to haemoglobinopathy1162327000
- Avascular necrosis of bone of foot due to hemoglobinopathy1162327000
- Osteonecrosis of foot due to haemoglobinopathy1162327000
- Osteonecrosis of foot due to hemoglobinopathy1162327000
- Aseptic necrosis of bone of forearm due to haemoglobinopathy1162328005
- Aseptic necrosis of bone of forearm due to hemoglobinopathy1162328005
- Avascular necrosis of bone of forearm due to haemoglobinopathy1162328005
- Avascular necrosis of bone of forearm due to hemoglobinopathy1162328005
- Osteonecrosis of bone of forearm due to haemoglobinopathy1162328005
- Osteonecrosis of bone of forearm due to hemoglobinopathy1162328005
- Aseptic necrosis of femur due to haemoglobinopathy1162337005
- Aseptic necrosis of femur due to hemoglobinopathy1162337005
- Avascular necrosis of femur due to haemoglobinopathy1162337005
- Avascular necrosis of femur due to hemoglobinopathy1162337005
- Osteonecrosis of femur due to haemoglobinopathy1162337005
- Osteonecrosis of femur due to hemoglobinopathy1162337005
- Aseptic necrosis of bone of ankle joint region due to haemoglobinopathy1162340005
- Aseptic necrosis of bone of ankle joint region due to hemoglobinopathy1162340005
- Avascular necrosis of bone of ankle joint region due to haemoglobinopathy1162340005
- Avascular necrosis of bone of ankle joint region due to hemoglobinopathy1162340005
- Osteonecrosis of ankle due to haemoglobinopathy1162340005
- Osteonecrosis of ankle due to hemoglobinopathy1162340005
- Aseptic necrosis of bone of pelvic region due to haemoglobinopathy1162363000
- Aseptic necrosis of bone of pelvic region due to hemoglobinopathy1162363000
- Avascular necrosis of bone of pelvic region due to haemoglobinopathy1162363000
- Avascular necrosis of bone of pelvic region due to hemoglobinopathy1162363000
- Osteonecrosis of pelvic region due to haemoglobinopathy1162363000
- Osteonecrosis of pelvic region due to hemoglobinopathy1162363000
- Aseptic necrosis of bone of shoulder region due to haemoglobinopathy1162365007
- Aseptic necrosis of bone of shoulder region due to hemoglobinopathy1162365007
- Avascular necrosis of bone of shoulder region due to haemoglobinopathy1162365007
- Avascular necrosis of bone of shoulder region due to hemoglobinopathy1162365007
- Osteonecrosis of shoulder region due to haemoglobinopathy1162365007
- Osteonecrosis of shoulder region due to hemoglobinopathy1162365007
- Pseudoxanthoma elasticum due to haemoglobinopathy1254936009
- Pseudoxanthoma elasticum due to hemoglobinopathy1254936009
- Aseptic necrosis of pelvis1335735002
- Avascular necrosis of pelvis1335735002
- Osteonecrosis of pelvis1335735002
- Aseptic necrosis of humerus1335749006
- Avascular necrosis of humerus1335749006
- Osteonecrosis of humerus1335749006
- Haemoglobin Iraq-Halabja trait1365693009
- Hemoglobin Iraq-Halabja trait1365693009
UMLS
- Abnormal HbC0349705
- Abnormal haemoglobinC0349705
- Abnormal hemoglobinC0349705
- Abnormal hemoglobin NOSC0349705
- Haemoglobin NOS abnormalC0349705
- Haemoglobin abnormalC0349705
- Haemoglobin abnormal NOSC0349705
- Hemoglobin abnormalC0349705
- abnormal hemoglobinC0349705
- hemoglobin abnormalC0349705
- C Disease, HemoglobinC0019021
- C Diseases, HemoglobinC0019021
- HEMOGLOBIN C DISC0019021
- Haemoglobin C diseaseC0019021
- Haemoglobin C-C diseaseC0019021
- Hb-C diseaseC0019021
- Hemoglobin C DiseaseC0019021
- Hemoglobin C DiseasesC0019021
- Hemoglobin C diseaseC0019021
- Hemoglobin C disease (disorder)C0019021
- Hemoglobin C-C diseaseC0019021
- Hemoglobin-C DiseaseC0019021
- Hemoglobin-C DiseasesC0019021
- Homozygous for Hb CC0019021
- CHBHA - Congenital Heinz body haemolytic anaemiaC0272006
- CHBHA - Congenital Heinz body hemolytic anemiaC0272006
- Congenital Heinz body anaemiaC0272006
- Congenital Heinz body anemiaC0272006
- Congenital Heinz body haemolytic anaemiaC0272006
- Congenital Heinz body hemolytic anemiaC0272006
- Unstable haemoglobin diseaseC0272006
- Unstable hemoglobin diseaseC0272006
- Unstable hemoglobin disease (disorder)C0272006
- Unstable hemoglobin hemolytic diseaseC0272006
- Globin abnormalityC0019045
- Haemoglobin diseaseC0019045
- Haemoglobin disorderC0019045
- HaemoglobinopathiesC0019045
- Haemoglobinopathies congenitalC0019045
- HaemoglobinopathyC0019045
- Haemoglobinopathy NOSC0019045
- Hemoglobin diseaseC0019045
- Hemoglobin disorderC0019045
- HemoglobinopathiesC0019045
- Hemoglobinopathies / Iron MetabolismC0019045
- HemoglobinopathyC0019045
- Hemoglobinopathy (disorder)C0019045
- Hemoglobinopathy NOSC0019045
- diseases hemoglobinC0019045
- disorders hemoglobinC0019045
- haemoglobin diseaseC0019045
- haemoglobinopathiesC0019045
- haemoglobinopathyC0019045
- hemoglobin diseaseC0019045
- hemoglobin disorderC0019045
- hemoglobin disordersC0019045
- hemoglobinopathiesC0019045
- hemoglobinopathyC0019045
- Haemoglobin D diseaseC0272080
- Haemoglobin D-D diseaseC0272080
- Hb-D diseaseC0272080
- Hemoglobin D DiseaseC0272080
- Hemoglobin D diseaseC0272080
- Hemoglobin D disease (disorder)C0272080
- Hemoglobin D-D diseaseC0272080
- Sickle Cell-Hemoglobin D DiseaseC0272080
- Haemoglobin E diseaseC0238159
- Haemoglobin E-E diseaseC0238159
- Hb-E diseaseC0238159
- Hemoglobin E DiseaseC0238159
- Hemoglobin E diseaseC0238159
- Hemoglobin E disease (disorder)C0238159
- Hemoglobin E-E diseaseC0238159
- Homozygous for Hb EC0238159
- Homozygous haemoglobin EC0238159
- Homozygous hemoglobin EC0238159
- diseases e haemoglobinC0238159
- hemoglobin e diseaseC0238159
- Other haemoglobinopathiesC0029632
- Other hemoglobinopathiesC0029632
Frequently Asked Questions
What is ICD-10 code D58.2?
ICD-10-CM code D58.2 represents "Other hemoglobinopathies". It 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.
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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.