Premature arteriosclerosis
Symptom Information:
Symptom ID: | HPO:0005177 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Arteriosclerosis(HPO:0002634) Premature arteriosclerosis(HPO:0005177) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
CADASIL | (Orphanet:136) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Fish-eye disease | (Orphanet:79292) |
LCAT deficiency | (Orphanet:650) |
Werner syndrome | (Orphanet:902) |