Urinary bladder sphincter dysfunction

Symptom Information:

Symptom ID: HPO:0002839
Synonyms:
Sphincter disturbance [HPO:0002839]
Sphincter disturbances [HPO:0002839]
Sphincter disturbances [OMIM:Sphincter disturbances]
Quality:
Cross references:
OMIM: "Sphincter disturbances" [OMIM:Sphincter disturbances]
Is a (Direct Parents):
HPO         Functional abnormality of the bladder
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:
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)