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Disease association ontology term - MONDO:0019625 - familial thoracic aortic aneurysm and aortic dissection

Term summary

ID
MONDO:0019625
Name
familial thoracic aortic aneurysm and aortic dissection
Ontology or CV name
Disease association
Definition
A rare genetic vascular disease characterized by the familial occurrence of thoracic aortic aneurysm, dissection or dilatation affecting one or more aortic segments (aortic root, ascending aorta, arch or descending aorta) in the absence of any other associated disease. Depending on the size, location and progression rate of dilatation/dissection, patients may be asymptomatic or may present dyspnea, cough, jaw, neck, chest or back pain, head, neck or upper limb edema, difficulty swallowing, voice hoarseness, pale skin, faint pulse and/or numbness/tingling in limbs. Patients have increased risk of presenting life threatening aortic rupture.

Parents

Annotation

Disease association

MONDO:0007568 - aortic aneurysm, familial thoracic 4

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Genes:

MONDO:0012730 - aortic aneurysm, familial thoracic 6

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Genes: