Disease association ontology term - MONDO:0021181 - inherited blood coagulation disorder

Term summary

ID: MONDO:0021181
Name: inherited blood coagulation disorder
Ontology or CV name: Disease association
Definition: Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.

Parents

is_a blood coagulation disease
is_a hereditary disease

Annotation

Disease association

MONDO:0018794 - cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder

References:

PB_REF:0000006

Genes:

MONDO:0009206 - factor V and factor VIII, combined deficiency of, type 1

References:

PB_REF:0000006

Genes:

emp43 (SPBC4F6.05c)

MONDO:0014885 - Hermansky-Pudlak syndrome 10

References:

PB_REF:0000006

Genes:

apl5 (SPAC144.06)

MONDO:0011997 - Hermansky-Pudlak syndrome 2

References:

PB_REF:0000006

Genes:

apl6 (SPAC23H3.06)

MONDO:0012465 - hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency

References:

PB_REF:0000006

Genes:

gpi14 (SPBC13E7.05)

MONDO:0008559 - thrombophilia due to thrombin defect

References:

PB_REF:0000006

Genes:

MONDO:0010518 - Wiskott-Aldrich syndrome

References:

Genes: