Renal artery stenosis

Symptom Information:

Symptom ID: HPO:0001920
Synonyms:
Renal artery stenosis [OMIM:Renal artery stenosis]
Renal artery stenosis [MedDRA:10038378]
Quality:
Cross references:
OMIM: "Renal artery stenosis" [OMIM:Renal artery stenosis]
Is a (Direct Parents):
HPO         Arterial stenosis
MedDRA Renal vascular and ischaemic conditions
HPO         Abnormality of the renal artery
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal morphology(HPO:0012210)
                      Abnormality of the renal artery(HPO:0008776)
                         Renal artery stenosis(HPO:0001920)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Abnormalities of the peripheral arteries(HPO:0005114)
                   Arterial stenosis(HPO:0100545)
                      Renal artery stenosis(HPO:0001920)
                Abnormality of the renal artery(HPO:0008776)
                   Renal artery stenosis(HPO:0001920)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal vascular and ischaemic conditions(MedDRA:10038543)
          Renal artery stenosis(HPO:0001920)
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO (OMIM:171300)
Williams syndrome (Orphanet:904)