Microalbuminuria
Symptom Information:
Symptom ID: | HPO:0012594 | ||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of urine homeostasis(HPO:0003110) Proteinuria(HPO:0000093) Albuminuria(HPO:0012592) Microalbuminuria(HPO:0012594) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the urinary system(HPO:0000079) Abnormality of the urinary system physiology(HPO:0011277) Abnormality of urine homeostasis(HPO:0003110) Proteinuria(HPO:0000093) Albuminuria(HPO:0012592) Microalbuminuria(HPO:0012594) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Diabetic complications(MedDRA:10012653) Diabetic complications renal(MedDRA:10012658) Microalbuminuria(HPO:0012594) |
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Database Frequency: | 6 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Bardet-Biedl syndrome 17 | (OMIM:615994) |
Fabry disease | (Orphanet:324) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Maturity-onset diabetes of the young, type 3 | (OMIM:600496) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |