inherited blood coagulation disorder

Findings

No curated finding names inherited blood coagulation disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• blood coagulation disease
• hereditary disease

Narrower terms (40)

• alpha-2-plasmin inhibitor deficiency
• congenital factor V deficiency
• congenital factor XI deficiency
• congenital factor XII deficiency
• congenital high-molecular-weight kininogen deficiency
• congenital plasminogen activator inhibitor type 1 deficiency
• congenital thrombotic thrombocytopenic purpura
• congenital vitamin K-dependent coagulation factors deficiency
• cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
• dysplasminogenemia
• Ehlers-Danlos syndrome, fibronectinemic type
• factor 5 and Factor VIII, combined deficiency of, 2
• factor V and factor VIII, combined deficiency of, type 1
• factor VII and Factor VIII, combined deficiency of
• factor XIII, A subunit, deficiency of
• factor XIII, b subunit, deficiency of

Resolves to: inherited blood coagulation disorder

Also called

coagulation disorder, hereditarycoagulation disorder, inheritedcoagulation disorders, hereditarycoagulation disorders, inheritedhereditary blood coagulation diseasehereditary blood coagulation disordershereditary coagulation disorderhereditary coagulation disordersinherited blood coagulation disordersinherited coagulation disorderinherited coagulation disordersrare genetic coagulation disorder