Premature coronary artery disease

Symptom Information:

Symptom ID: HPO:0005181
Synonyms:
Coronary artery disease, premature [OMIM:Coronary artery disease, premature]
Quality:
Cross references:
OMIM: "Coronary artery disease, premature" [OMIM:Coronary artery disease, premature]
Is a (Direct Parents):
HPO         Coronary artery disease
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)
                   Coronary artery disease(HPO:0001677)
                      Premature coronary artery disease(HPO:0005181)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Abnormalities of the peripheral arteries(HPO:0005114)
                   Arterial stenosis(HPO:0100545)
                      Coronary artery disease(HPO:0001677)
                         Premature coronary artery disease(HPO:0005181)
                Abnormality of the coronary arteries(HPO:0006704)
                   Coronary artery disease(HPO:0001677)
                      Premature coronary artery disease(HPO:0005181)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

AORTIC ANEURYSM, FAMILIAL THORACIC 6 (OMIM:611788)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Tangier disease (Orphanet:31150)