Hyposthenuria

Symptom Information:

Symptom ID: HPO:0003158
Synonyms:
Reduced urinary osmolality [HPO:0003158]
Hyposthenuria [OMIM:Hyposthenuria]
Hyposthenuria (inability to concentrate urine normally) [OMIM:Hyposthenuria (inability to concentrate urine normally)]
Hyposthenuria [MedDRA:10021096]
Quality:
Cross references:
OMIM: "Hyposthenuria" [OMIM:Hyposthenuria]
OMIM: "Hyposthenuria (inability to concentrate urine normally)" [OMIM:Hyposthenuria (inability to concentrate urine normally)]
UMLS:C0232831 "Hyposthenuria" [HPO:0003158]
Is a (Direct Parents):
HPO         Abnormality of urine homeostasis
MedDRA Urinary abnormalities
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)