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Disease association ontology term - MONDO:0005385 - vascular disorder

Term summary

ID
MONDO:0005385
Name
vascular disorder
Ontology or CV name
Disease association
Definition
A general term used to describe any disease affecting blood vessels]. It includes vascular abnormalities caused by degenerative, metabolic and inflammatory conditions, embolic diseases, coagulative disorders, and functional disorders such as posteri or reversible encephalopathy syndrome.

Parents

Annotation

Disease association

MONDO:0007568 - aortic aneurysm, familial thoracic 4

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MONDO:0012730 - aortic aneurysm, familial thoracic 6

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MONDO:0018870 - arterial calcification of infancy

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MONDO:0013768 - arterial calcification, generalized, of infancy, 2

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MONDO:0007154 - arteriovenous malformations of the brain

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MONDO:0979873 - brain small vessel disease 4

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MONDO:0980711 - brain small vessel disease 6 with leukoencephalopathy

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MONDO:0010829 - CARASIL syndrome

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MONDO:0014768 - cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2

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MONDO:0013644 - Charcot-Marie-Tooth disease axonal type 2O

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MONDO:0010557 - choroideremia

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MONDO:0012011 - coronary artery disease, autosomal dominant, 1

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MONDO:0007781 - essential hypertension, genetic

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MONDO:0013806 - familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

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MONDO:0007672 - glomuvenous malformation

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MONDO:0008895 - hereditary arterial and articular multiple calcification syndrome

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MONDO:0013458 - hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome

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MONDO:0013805 - intellectual disability, autosomal dominant 13

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MONDO:0007918 - microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability

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MONDO:0013542 - Moyamoya disease 5

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MONDO:0011257 - MPI-congenital disorder of glycosylation

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MONDO:0013452 - multisystemic smooth muscle dysfunction syndrome

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MONDO:0018997 - Noonan syndrome

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MONDO:0033669 - Noonan syndrome 13

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MONDO:0012371 - Noonan syndrome 3

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MONDO:0013186 - Noonan syndrome 6

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MONDO:0009796 - ornithine aminotransferase deficiency

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MONDO:0009935 - pulmonary hypertension, primary, 5

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MONDO:0009937 - pulmonary venoocclusive disease

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MONDO:0009329 - pulmonary venoocclusive disease 2

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