Congenital sideroblastic anaemias

Description

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 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.

Exclusions from above levels

04 – Diseases of the immune system
05 – Endocrine, nutritional or metabolic diseases
18 – Complications of pregnancy, childbirth or the puerperium

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19 – Certain conditions originating in the perinatal period
20 – Congenital malformations, deformations or chromosomal abnormalities
22 – Injury, poisoning or certain other consequences of external causes
http://id.who.int/icd/entity/1000704511 – Human immunodeficiency virus disease
JB64.1 – Other diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism complicating pregnancy, childbirth or the puerperium

Child codes

3A72.00 – Hereditary sideroblastic anaemias
3A72.01 – Hereditary syndromic sideroblastic anaemia
3A72.0Y – Other specified congenital sideroblastic anaemias
3A72.0Z – Congenital sideroblastic anaemias, unspecified

Sibling codes

3A72.1 – Acquired sideroblastic anaemias
3A72.Z – Sideroblastic anaemia, unspecified

Foundation entity

Congenital sideroblastic anaemias – http://id.who.int/icd/entity/1090108163

Part of: 3A72: Sideroblastic anaemia › 03: Diseases of the blood or blood-forming organs