Haemoglobin C disease

ICD-11 code : 3A51.5;

Preferred Label : Haemoglobin C disease;

ICD-11 definition : A disease caused by the bi-parental gene that encodes for haemoglobin C. This disease is characterised by abnormal structure of one of the globin chains of the haemoglobin molecule. This disease may present with mild haemolytic anaemia, increased risk for gallstones, enlarged spleen, episodes of joint pain, and increased risk of infection. This disease is confirmed by identification of the haemoglobin C gene by genetic testing.;

ICD-11 inclusion : Homozygous (HbC/HbC, HbC/beta-thal and other);

Details

Origin ID

2097316574;

UMLS CUI

C0019021;

Currated CISMeF NLP mapping
- Haemoglobin C disease [MedDRA Preferred Term]
- Hemoglobin C Disease [NCIt concept]
- Hemoglobin C disease [MedDRA LLT]
- Hemoglobin C disease [ORDO Disease]
- Hemoglobin C disease (disorder) [SNOMED CT concept]
- hemoglobin C disease [DO Concept]
- hemoglobin C disease [Disease (Nov.)]
- hemoglobin C disease [MeSH concept]
- hemoglobin c disease [MeSH Descriptor]
- hemoglobin c disease [SNOMED Notion]
ICD-10 Mapping
- Sickle-cell disorders [ICD-10 category]
See also inter- (CISMeF)
- Sickle cell-hemoglobin SS disease (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Haemoglobin C disease [MedDRA Preferred Term]
- Hemoglobin C Disease [NCIt concept]
- Hemoglobin C disease [MedDRA LLT]
- Hemoglobin C disease [ORDO Disease]
- Hemoglobin C disease (disorder) [SNOMED CT concept]
- hemoglobin C disease [DO Concept]
- hemoglobin C disease [MeSH concept]
- hemoglobin C disease [Disease (Nov.)]
- hemoglobin c disease [MeSH Descriptor]
- hemoglobin c disease [SNOMED Notion]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients