Urinary incontinence
Symptom Information:
| Symptom ID: | HPO:0000020 | |||||||||
| Synonyms: |
|
|||||||||
| Quality: | ||||||||||
| Cross references: |
|
|||||||||
| Is a (Direct Parents): |
|
|||||||||
| 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 incontinence(HPO:0000020) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Bladder and urethral symptoms(MedDRA:10004995) Urinary incontinence(HPO:0000020) |
|||||||||
| Database Frequency: | 75 / 7739 | |||||||||
| Resource: |
All diseases associated with this symptom:
| 3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
| AMYOTROPHIC DYSTONIC PARAPLEGIA | (OMIM:105300) |
| APNEA, CENTRAL SLEEP | (OMIM:207720) |
| ATTRV122I amyloidosis | (Orphanet:85451) |
| Acute intermittent porphyria | (Orphanet:79276) |
| Adrenomyeloneuropathy | (Orphanet:139399) |
| Adult polyglucosan body disease | (Orphanet:206583) |
| Alström syndrome | (Orphanet:64) |
| Arnold-Chiari malformation type I | (Orphanet:268882) |
| 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 36 | (Orphanet:320365) |
| Autosomal dominant spastic paraplegia type 37 | (Orphanet:171612) |
| 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 dominant spastic paraplegia type 9 | (Orphanet:100990) |
| Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
| Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
| Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
| Autosomal recessive spastic paraplegia type 44 | (Orphanet:320401) |
| Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
| Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
| Autosomal recessive spastic paraplegia type 54 | (Orphanet:320380) |
| Autosomal recessive spastic paraplegia type 5A | (Orphanet:100986) |
| Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
| BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 | (OMIM:213600) |
| Bardet-Biedl syndrome 10 | (OMIM:615987) |
| Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
| Bilateral striopallidodentate calcinosis | (Orphanet:1980) |
| CADASIL | (Orphanet:136) |
| CAMOS syndrome | (Orphanet:83472) |
| CARASIL | (Orphanet:199354) |
| Camptobrachydactyly | (Orphanet:1319) |
| Charcot-Marie-Tooth disease type 4B3 | (Orphanet:363981) |
| Christianson syndrome | (Orphanet:85278) |
| Citrullinemia type II | (Orphanet:247585) |
| Currarino triad | (Orphanet:1552) |
| Familial amyloid polyneuropathy | (Orphanet:85447) |
| Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
| Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
| Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
| HYDROCEPHALUS, NORMAL-PRESSURE | (OMIM:236690) |
| Huntington disease-like 3 | (Orphanet:157946) |
| Infantile-onset ascending hereditary spastic paralysis | (Orphanet:293168) |
| Leber plus disease | (Orphanet:99718) |
| METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
| METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY | (OMIM:249900) |
| MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO | (OMIM:126200) |
| Metachromatic leukodystrophy | (Orphanet:512) |
| Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
| Multiple system atrophy | (Orphanet:102) |
| NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO | (OMIM:182940) |
| NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB | (OMIM:613115) |
| Nasu-Hakola disease | (Orphanet:2770) |
| Neural tube closure defect | (Orphanet:268357) |
| Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
| Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
| Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
| SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION | (OMIM:607565) |
| SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 | (OMIM:604320) |
| Sandhoff disease, infantile form | (Orphanet:309155) |
| Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |
| Spinocerebellar ataxia type 10 | (Orphanet:98761) |
| Spinocerebellar ataxia type 17 | (Orphanet:98759) |
| Syringomyelia | (Orphanet:3280) |
| 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) |