Hereditary factor VIII deficiency

Description

A disease caused by a genetically inherited mutation leading to a deficiency in clotting due to lack of factor VIII. This disease is characterised by increasing haemorrhaging and bruising. Confirmation is by identification of mutations by genetic testing.

Exclusions from above levels

JA43.3 – Postpartum coagulation defects
04 – Diseases of the immune system
05 – Endocrine, nutritional or metabolic diseases

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18 – Complications of pregnancy, childbirth or the puerperium
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

3B10.0 – Haemophilia A
3B10.1 – Hereditary factor VIII deficiency with anti-factor VIII inhibitor
3B10.Y – Other specified hereditary factor VIII deficiency
3B10.Z – Hereditary factor VIII deficiency, unspecified

Sibling codes

3B11 – Hereditary factor IX deficiency
3B12 – Von Willebrand disease
3B13 – Haemophilia C
3B14 – Other inherited coagulation factor deficiency with bleeding tendency
3B15 – Inherited coagulation factor deficiency without bleeding tendency
3B1Z – Congenital or constitutional haemorrhagic condition, unspecified

Foundation entity

Hereditary factor VIII deficiency – http://id.who.int/icd/entity/1573164739

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