Atherosclerosis

Symptom Information:

Symptom ID: HPO:0002621
Synonyms:
Atherosclerosis (morphologic abnormality) [Orphanet:35510]
Atheroma (morphologic abnormality) [Orphanet:35510]
Atheroma of artery (disorder) [Orphanet:35510]
Atheroma [Orphanet:35510]
Atherosclerosis [Orphanet:35510]
Atherosclerosis [OMIM:Atherosclerosis]
Arterial atheroma/precocious atherosclerosis/arteriosclerosis [Orphanet:35510]
Atheromatosis [Orphanet:35510]
Arteriosclerosis [MedDRA:10003210]
Atherosclerosis [MedDRA:10003210]
Atherosclerosis generalized [MedDRA:10003210]
Atherosclerosis of other specified arteries [MedDRA:10003210]
Generalized and unspecified atherosclerosis [MedDRA:10003210]
Generalized arteriosclerosis [MedDRA:10003210]
Generalized atheroma [MedDRA:10003210]
Hyperplastic atherosclerosis [MedDRA:10003210]
Nodular atherosclerosis [MedDRA:10003210]
Atheroma [MedDRA:10003210]
Arteriosclerotic cardiovascular disease [MedDRA:10003210]
Atherosclerotic cardiovascular disease [MedDRA:10003210]
Vascular atheroma [MedDRA:10003210]
Atheromatosis [MedDRA:10003210]
Atherosclerosis generalised [MedDRA:10003210]
Generalised arteriosclerosis [MedDRA:10003210]
Generalised atheroma [MedDRA:10003210]
Quality:
Cross references:
Orphanet:35510 "Arterial atheroma/precocious atherosclerosis/arteriosclerosis" [Orphanet:35510]
OMIM: "Atherosclerosis" [OMIM:Atherosclerosis]
UMLS:C0004153 "Atherosclerosis" [HPO:0002621]
UMLS:C0264956 "Atheroma" [Orphanet:35510]
UMLS:C0004153 "Atherosclerosis" [Orphanet:35510]
Is a (Direct Parents):
Orphanet Abnormality of cardiovascular system physiology
HPO         Arteriosclerosis
MedDRA Non-site specific necrosis and vascular insufficiency NEC
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)
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)