Renovascular hypertension
Symptom Information:
Symptom ID: | HPO:0100817 | |||||||||||||||||||||||||
Synonyms: |
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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 cardiovascular system physiology(HPO:0011025) Hypertension(HPO:0000822) Renovascular hypertension(HPO:0100817) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the urinary system(HPO:0000079) Abnormality of the urinary system physiology(HPO:0011277) Abnormal renal physiology(HPO:0012211) Renovascular hypertension(HPO:0100817) Abnormality of the upper urinary tract(HPO:0010935) Abnormality of the kidney(HPO:0000077) Abnormal renal physiology(HPO:0012211) Renovascular hypertension(HPO:0100817) MedDRA: Vascular disorders(MedDRA:10047065) Vascular hypertensive disorders(MedDRA:10057166) Renovascular hypertension(HPO:0100817) Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal hypertension and related conditions(MedDRA:10038466) Renovascular hypertension(HPO:0100817) |
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Database Frequency: | 9 / 7739 | |||||||||||||||||||||||||
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All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Fibromuscular dysplasia of arteries | (Orphanet:336) |
Hypophosphatemic rickets, autosomal recessive, 2 | (OMIM:613312) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Williams syndrome | (Orphanet:904) |
[DEL] PSEUDOXANTHOMA ELASTICUM | (OMIM:264800) |