3B14
Other inherited coagulation factor deficiency with bleeding tendency
Outra deficiência hereditária de fator da coagulação com tendência hemorrágica
CategoryDefinition
Any disease caused by genetically inherited mutations leading to lack of coagulation factors in the blood not elsewhere classified. These diseases are characterised by increased haemorrhaging and bruising as the blood cannot clot properly to control bleeding. Confirmation is identification of mutations by genetic testing.