Pollakisuria
Symptom Information:
Symptom ID: | HPO:0100515 | |||||||||||||||||||||
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 lower urinary tract(HPO:0010936) Abnormality of the bladder(HPO:0000014) Functional abnormality of the bladder(HPO:0000009) Pollakisuria(HPO:0100515) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Bladder and urethral symptoms(MedDRA:10004995) Pollakisuria(HPO:0100515) |
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Database Frequency: | 12 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Alström syndrome | (Orphanet:64) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Caudal regression sequence | (Orphanet:3027) |
Cushing syndrome | (Orphanet:553) |
Cystinosis | (Orphanet:213) |
Familial caudal dysgenesis | (Orphanet:1768) |
MELAS | (Orphanet:550) |
Nephronophthisis 1 | (OMIM:256100) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Sirenomelia | (Orphanet:3169) |