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Disease association ontology term - MONDO:0002243 - hemorrhagic disease

Term summary

ID
MONDO:0002243
Name
hemorrhagic disease
Ontology or CV name
Disease association
Definition
Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (blood coagulation disorders) or another abnormality causing a structural flaw in the blood vessels (hemostatic disorders).

Parents

Annotation

Disease association

MONDO:0957580 - bleeding disorder, platelet-type, 25

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Genes:

MONDO:0018175 - combined deficiency of factor V and factor VIII

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Genes:

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

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Genes:

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

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MONDO:0015912 - macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss

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Genes:

MONDO:0014078 - platelet-type bleeding disorder 15

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Genes:

MONDO:0014518 - platelet-type bleeding disorder 19

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Genes: