Renal steatosis
Symptom Information:
Symptom ID: | HPO:0000799 | |||
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 morphology(HPO:0012210) Renal steatosis(HPO:0000799) MedDRA: |
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Database Frequency: | 6 / 7739 | |||
Resource: |
All diseases associated with this symptom:
BOR syndrome | (Orphanet:107) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Phosphoenolpyruvate carboxykinase 1 deficiency | (Orphanet:79316) |
Phosphoenolpyruvate carboxykinase 2 deficiency | (Orphanet:79317) |
Phosphoenolpyruvate carboxykinase deficiency | (Orphanet:2880) |
VISCERAL STEATOSIS, CONGENITAL | (OMIM:228100) |