Urinary urgency

Symptom Information:

Symptom ID: HPO:0000012
Synonyms:
Overactive bladder syndrome [HPO:0000012]
Urgency frequency syndrome [HPO:0000012]
Urinary urgency [OMIM:Urinary urgency]
Urinary urgency (57%) [OMIM:Urinary urgency (57%)]
Urinary urgency (in 44% of patients) [OMIM:Urinary urgency (in 44% of patients)]
Urinary urgency (in some patients) [OMIM:Urinary urgency (in some patients)]
Urinary urgency (less common) [OMIM:Urinary urgency (less common)]
Quality:
Cross references:
OMIM: "Urinary urgency" [OMIM:Urinary urgency]
OMIM: "Urinary urgency (57%)" [OMIM:Urinary urgency (57%)]
OMIM: "Urinary urgency (in 44% of patients)" [OMIM:Urinary urgency (in 44% of patients)]
OMIM: "Urinary urgency (in some patients)" [OMIM:Urinary urgency (in some patients)]
OMIM: "Urinary urgency (less common)" [OMIM:Urinary urgency (less common)]
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 urgency(HPO:0000012)
MedDRA:
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

Adult polyglucosan body disease (Orphanet:206583)
Alström syndrome (Orphanet:64)
Autosomal dominant Charcot-Marie-Tooth disease type 2C (Orphanet:99937)
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 29 (Orphanet:101009)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Autosomal dominant spastic paraplegia type 31 (Orphanet:101011)
Autosomal dominant spastic paraplegia type 36 (Orphanet:320365)
Autosomal dominant spastic paraplegia type 37 (Orphanet:171612)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal dominant spastic paraplegia type 41 (Orphanet:320355)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Autosomal dominant spastic paraplegia type 8 (Orphanet:100989)
Autosomal dominant spastic paraplegia type 9 (Orphanet:100990)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (Orphanet:98)
Autosomal recessive spastic ataxia with leukoencephalopathy (Orphanet:314603)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 26 (Orphanet:101006)
Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
Autosomal recessive spastic paraplegia type 7 (Orphanet:99013)
METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA (OMIM:156310)
Metachromatic leukodystrophy (Orphanet:512)
Multiple system atrophy (Orphanet:102)
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:605909)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION (OMIM:607565)
Spinocerebellar ataxia type 10 (Orphanet:98761)
Spinocerebellar ataxia type 25 (Orphanet:101111)
X-linked spastic paraplegia type 16 (Orphanet:100997)
Young adult-onset Parkinsonism (Orphanet:2828)
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE (OMIM:607259)