Urinary bladder sphincter dysfunction
Symptom Information:
Symptom ID: | HPO:0002839 | |||
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) Urinary bladder sphincter dysfunction(HPO:0002839) MedDRA: |
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Database Frequency: | 34 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Adult polyglucosan body disease | (Orphanet:206583) |
Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
Alexander disease | (Orphanet:58) |
Arachnoiditis | (Orphanet:137817) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 12 | (Orphanet:100993) |
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 19 | (Orphanet:100999) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal dominant spastic paraplegia type 8 | (Orphanet:100989) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 30 | (Orphanet:101010) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Caudal regression sequence | (Orphanet:3027) |
Cobb syndrome | (Orphanet:53721) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Friedreich ataxia 1 | (OMIM:229300) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Isolated spina bifida | (Orphanet:823) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE | (OMIM:615625) |
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION | (OMIM:607565) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Williams syndrome | (Orphanet:904) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |
X-linked spastic paraplegia type 16 | (Orphanet:100997) |
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE | (OMIM:607259) |