Aplastic anaemia

Description

A disease caused by determinants arising after birth, in the antenatal period or genetically inherited factors leading to the inability of stem cells to generate new mature cells. This disease is characterised by low levels of red blood cells, white blood cells, and platelets. This disease may present with pallor, fatigue, dizziness, increased risk of infection or increased bruising or bleeding.

Inclusions

Medullary hypoplasia
Panmyelophthisis

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

3A70.0 – Congenital aplastic anaemia
3A70.1 – Acquired aplastic anaemias
3A70.Z – Aplastic anaemia, unspecified

Sibling codes

3A50 – Thalassaemias
3A51 – Sickle cell disorders or other haemoglobinopathies
3A71 – Anaemia due to chronic disease
3A72 – Sideroblastic anaemia
3A73 – Congenital dyserythropoietic anaemia
3A90 – Anaemia due to acute disease
3A91 – Congenital methaemoglobinaemia
3A92 – Hereditary methaemoglobinaemia
3A93 – Acquired methaemoglobinaemia
3A94 – Acute posthaemorrhagic anaemia
3A9Y – Other specified anaemias or erythrocyte disorders
3A9Z – Anaemias or other erythrocyte disorders, unspecified

Foundation entity

Aplastic anaemia – http://id.who.int/icd/entity/502834133

Part of: 03: Diseases of the blood or blood-forming organs