Polyuria
Symptom Information:
Symptom ID: | HPO:0000103 | ||||||||||||||||||
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 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: Investigations(MedDRA:10022891) Renal and urinary tract investigations and urinalyses(MedDRA:10038362) Urinary tract function analyses NEC(MedDRA:10049179) Polyuria(HPO:0000103) Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Urinary tract signs and symptoms NEC(MedDRA:10046591) Polyuria(HPO:0000103) |
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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) |