Congenital sideroblastic anaemias

ICD-11 code : 3A72.0;

Preferred Label : Congenital sideroblastic anaemias;

ICD-11 definition : A disease caused by determinants arising in the antenatal period leading to the production of ringed sideroblasts; abnormal nucleated erythroblasts. This disease is characterised by the inability of to incorporate haemoglobin, which red blood cells need to transport oxygen efficiently. This disease may present with pallor, fatigue, dizziness, and enlarged spleen and liver, heart disease, liver damage, or kidney failure.;

ICD-11 "other" category code : 3A72.0Y;

ICD-11 "unspecified" category code : 3A72.0Z;

Details

Origin ID

1090108163;

Automatic exact mappings (from CISMeF team)
- Congenital anomaly of blood, blood-forming organs and immune system [ICPC-3 diagnosis]
ICD-10 Mapping
- Other anemias [ICD-10 category]
Validated automatic mappings to BTNT
- Autosomal recessive sideroblastic anemia [ORDO Disease]
- Hereditary Sideroblastic Anemia [NCIt concept]
- Hereditary sideroblastic anaemia [MedDRA Preferred Term]
- Hereditary sideroblastic anaemia [ICD-10 Sub-category (who)]
- Hereditary sideroblastic anemia [MedDRA LLT]
- Hereditary sideroblastic anemia (disorder) [Inactive SNOMED CT concept]
- X-linked sideroblastic anemia [MeSH Supplementary Concept]
- hereditary sideroblastic anemia, nos [SNOMED Notion]
Validated automatic mappings to NTBT
- Other anemias [ICD-10 category]

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