Hyposthenuria
Symptom Information:
Symptom ID: | HPO:0003158 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of urine homeostasis(HPO:0003110) Hyposthenuria(HPO:0003158) 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) Hyposthenuria(HPO:0003158) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Urinary abnormalities(MedDRA:10000196) Hyposthenuria(HPO:0003158) |
||||
Database Frequency: | 6 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive medullary cystic kidney disease | (Orphanet:655) |
BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
Bartter syndrome | (Orphanet:112) |
Fabry disease | (Orphanet:324) |
Nephronophthisis 1 | (OMIM:256100) |