Abnormality of renal resorption
Symptom Information:
Symptom ID: | HPO:0011038 | ||||||||||||||||
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 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 physiology(HPO:0012211) Abnormality of renal resorption(HPO:0011038) Abnormality of the urinary system physiology(HPO:0011277) Abnormal renal physiology(HPO:0012211) Abnormality of renal resorption(HPO:0011038) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Nephropathies and tubular disorders NEC(MedDRA:10029150) Abnormality of renal resorption(HPO:0011038) |
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Database Frequency: | 6 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Cystinosis | (Orphanet:213) |
Fanconi renotubular syndrome 1 | (OMIM:134600) |
Glycogen storage disease due to GLUT2 deficiency | (Orphanet:2088) |
MELAS | (Orphanet:550) |
Wilson disease | (Orphanet:905) |