Acquired pyridoxine deficiency anaemia

Description

A disease caused by determinants arising after birth. This disease is characterised by low levels of pyridoxine (vitamin B6) leading to low levels of red blood cells in the body. This disease may present with fatigue, muscle weakness, loss of appetite, weight loss, diarrhoea, nausea, fast heartbeat or numbness in extremities. Confirmation is by identification of low levels of pyridoxine and low red blood cell count in a blood sample.

Index terms

Acquired pyridoxine deficiency anaemia
Acquired vitamin B6 deficiency anaemia

Exclusions from above levels

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

Show allHide

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

Sibling codes

3A03.41 – Acquired riboflavin deficiency anaemia
3A03.42 – Acquired thiamine deficiency anaemia
3A03.4Y – Other specified acquired other vitamin B deficiency anaemia

Foundation entity

Acquired pyridoxine deficiency anaemia – http://id.who.int/icd/entity/1119769670

Part of: 3A03.4: Acquired other vitamin B deficiency anaemia › 3A03: Certain nutritional or metabolic anaemias › 03: Diseases of the blood or blood-forming organs