Albuminuria
Symptom Information:
Symptom ID: | HPO:0012592 | ||||
Synonyms: |
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Cross references: |
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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) 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) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Urinary abnormalities(MedDRA:10000196) Albuminuria(HPO:0012592) |
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Database Frequency: | 6 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Limited systemic sclerosis | (Orphanet:220407) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
Zellweger syndrome | (Orphanet:912) |