Atherosclerosis
Symptom Information:
Symptom ID: | HPO:0002621 | |||||||||||||||||||||||||
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) Atherosclerosis(HPO:0002621) MedDRA: Vascular disorders(MedDRA:10047065) Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216) Non-site specific necrosis and vascular insufficiency NEC(MedDRA:10029558) Atherosclerosis(HPO:0002621) |
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Database Frequency: | 33 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
APOLIPOPROTEIN(a) | (OMIM:152200) |
Alkaptonuria | (Orphanet:56) |
Alström syndrome | (Orphanet:64) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency | (Orphanet:91135) |
CADASIL | (Orphanet:136) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis | (Orphanet:94062) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
Familial LCAT deficiency | (Orphanet:79293) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Fish-eye disease | (Orphanet:79292) |
Flynn-Aird syndrome | (Orphanet:2047) |
GAPO syndrome | (Orphanet:2067) |
HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE | (OMIM:603813) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hypoalphalipoproteinemia | (Orphanet:31153) |
LCAT deficiency | (Orphanet:650) |
LMNA-related cardiocutaneous progeria syndrome | (Orphanet:363618) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
Mediterranean macrothrombocytopenia | (Orphanet:101022) |
Nestor-Guillermo progeria syndrome | (Orphanet:280576) |
Odontomatosis - aortae esophagus stenosis | (Orphanet:2724) |
Primary lipodystrophy | (Orphanet:90970) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Sitosterolemia | (Orphanet:2882) |
TRAPS syndrome | (Orphanet:32960) |
Tangier disease | (Orphanet:31150) |
Werner syndrome | (Orphanet:902) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |