Renal cortical atrophy
Symptom Information:
Symptom ID: | HPO:0002048 | ||||
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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 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 cortex(HPO:0011035) Renal cortical atrophy(HPO:0002048) Renal atrophy(HPO:0012585) Renal cortical atrophy(HPO:0002048) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
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All diseases associated with this symptom:
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia | (Orphanet:34149) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |