Polyuria

Symptom Information:

Symptom ID: HPO:0000103
Synonyms:
Increased urine output [HPO:0000103]
Polyuria (finding) [Orphanet:38680]
Polyuric state (disorder) [Orphanet:38680]
Polyuria [Orphanet:38680]
Polyuria [OMIM:Polyuria]
Pollakiuria/polyuria/dysuria/anuria/acute urine retention/oliguria [Orphanet:38680]
Polyuria [MedDRA:10036142]
Diuresis [MedDRA:10036142]
Diuresis excessive [MedDRA:10036142]
Frequency of urination and polyuria [MedDRA:10036142]
Diuretic effect [MedDRA:10036142]
Polyuria (in some) [OMIM:Polyuria (in some)]
Acute retention of urine [MedDRA:10001055]
Acute urine retention [Orphanet:38680]
Acute retention of urine (disorder) [Orphanet:38680]
Bladder retention of urine (observable entity) [Orphanet:38680]
Acute retention of urine [Orphanet:38680]
Urine output increased [MedDRA:10059896]
Quality:
Cross references:
Orphanet:38680 "Pollakiuria/polyuria/dysuria/anuria/acute urine retention/oliguria" [Orphanet:38680]
OMIM: "Polyuria" [OMIM:Polyuria]
OMIM: "Polyuria (in some)" [OMIM:Polyuria (in some)]
UMLS:C0032617 "Polyuria" [HPO:0000103]
UMLS:C0032617 "Polyuria" [Orphanet:38680]
UMLS:C0341742 "Acute retention of urine" [Orphanet:38680]
Is a (Direct Parents):
MedDRA Urinary tract signs and symptoms NEC
HPO         Abnormal urine output
MedDRA Urinary tract function analyses NEC
Orphanet Abnormality of the urinary system physiology
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 urinary system physiology(HPO:0011277)
                Abnormal renal physiology(HPO:0012211)
                   Abnormality of renal excretion(HPO:0011036)
                      Abnormal urine output(HPO:0012590)
                         Polyuria(HPO:0000103)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Abnormality of renal excretion(HPO:0011036)
                         Abnormal urine output(HPO:0012590)
                            Polyuria(HPO:0000103)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Urinary tract signs and symptoms(MedDRA:10046590)
       Urinary tract signs and symptoms NEC(MedDRA:10046591)
          Polyuria(HPO:0000103)
Investigations(MedDRA:10022891)
    Renal and urinary tract investigations and urinalyses(MedDRA:10038362)
       Urinary tract function analyses NEC(MedDRA:10049179)
          Polyuria(HPO:0000103)
Database Frequency: 60 / 7739
Resource:

All diseases associated with this symptom:

Aceruloplasminemia (Orphanet:48818)
Alström syndrome (Orphanet:64)
Amelogenesis imperfecta - nephrocalcinosis (Orphanet:1031)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Autosomal recessive infantile hypercalcemia (Orphanet:300547)
Autosomal recessive medullary cystic kidney disease (Orphanet:655)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
BARTTER SYNDROME, TYPE 4A (OMIM:602522)
BARTTER SYNDROME, TYPE 4B (OMIM:613090)
Bardet-Biedl syndrome 17 (OMIM:615994)
Bartter syndrome (Orphanet:112)
Blue diaper syndrome (Orphanet:94086)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Classic Bartter syndrome (Orphanet:93605)
Cushing syndrome (Orphanet:553)
Cystinosis (Orphanet:213)
DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL (OMIM:125800)
DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED (OMIM:304800)
DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE (OMIM:304900)
DIABETES MELLITUS, INSULIN-DEPENDENT (OMIM:222100)
Dent disease type 1 (Orphanet:93622)
EAST syndrome (Orphanet:199343)
Fabry disease (Orphanet:324)
Familial hyperaldosteronism type 3 (Orphanet:251274)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Fanconi renotubular syndrome 1 (OMIM:134600)
Gitelman syndrome (Orphanet:358)
HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES (OMIM:239350)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
Infantile Bartter syndrome with deafness (Orphanet:89938)
Insulin-resistance syndrome type A (Orphanet:2297)
Joubert syndrome 5 (OMIM:610188)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
Maturity-onset diabetes of the young, type 4 (OMIM:606392)
Maturity-onset diabetes of the young, type 9 (OMIM:612225)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Nephrogenic diabetes insipidus (Orphanet:223)
Nephronophthisis 1 (OMIM:256100)
Nephronophthisis 2 (OMIM:602088)
Nephronophthisis 3 (OMIM:604387)
Nephronophthisis 4 (OMIM:606966)
Nephronophthisis 9 (OMIM:613824)
Primary Fanconi syndrome (Orphanet:3337)
Proximal renal tubular acidosis (Orphanet:47159)
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia (Orphanet:3390)
Rabson-Mendenhall syndrome (Orphanet:769)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renal glucosuria (Orphanet:69076)
Senior-Boichis syndrome (Orphanet:84081)
Senior-Loken syndrome (Orphanet:3156)
Senior-Loken syndrome 1 (OMIM:266900)
Senior-Loken syndrome 3 (OMIM:606995)
Senior-Loken syndrome 4 (OMIM:606996)
Senior-Loken syndrome 5 (OMIM:609254)
Senior-Loken syndrome 6 (OMIM:610189)
TERATOMA, PINEAL (OMIM:273120)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome 2 (OMIM:604928)