Bowel incontinence

Symptom Information:

Symptom ID: HPO:0002607
Synonyms:
Anal incontinence [HPO:0002607]
Encopresis [HPO:0002607]
Fecal incontinence [HPO:0002607]
Encopresis [Orphanet:27450]
Anal incontinence [Orphanet:27450]
Encopresis (finding) [Orphanet:27450]
Bowel incontinence [OMIM:Bowel incontinence]
Encopresis [OMIM:Encopresis]
Fecal incontinence [OMIM:Fecal incontinence]
Encopresis/fecal incontinence [Orphanet:27450]
Encopresis [MedDRA:10014643]
Fecal incontinence (never achieved) [OMIM:Fecal incontinence (never achieved)]
Fecal incontinence (rare) [OMIM:Fecal incontinence (rare)]
Quality:
Cross references:
Orphanet:27450 "Encopresis/fecal incontinence" [Orphanet:27450]
OMIM: "Bowel incontinence" [OMIM:Bowel incontinence]
OMIM: "Encopresis" [OMIM:Encopresis]
OMIM: "Fecal incontinence" [OMIM:Fecal incontinence]
OMIM: "Fecal incontinence (never achieved)" [OMIM:Fecal incontinence (never achieved)]
OMIM: "Fecal incontinence (rare)" [OMIM:Fecal incontinence (rare)]
UMLS:C2945606 "Encopresis (finding)" [Orphanet:27450]
Is a (Direct Parents):
HPO         Encopresis
MedDRA Psychiatric elimination disorders
HPO         Abnormality of the large intestine
Orphanet Functional anomalies of the digestive system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Abnormality of the intestine(HPO:0002242)
                   Abnormality of the large intestine(HPO:0002250)
                      Bowel incontinence(HPO:0002607)
MedDRA:
Database Frequency: 33 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
AMYOTROPHIC DYSTONIC PARAPLEGIA (OMIM:105300)
ANAL SPHINCTER DYSPLASIA (OMIM:105563)
Adrenomyeloneuropathy (Orphanet:139399)
Alexander disease (Orphanet:58)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 54 (Orphanet:320380)
Bladder exstrophy (Orphanet:93930)
CAMOS syndrome (Orphanet:83472)
Caudal regression sequence (Orphanet:3027)
Christianson syndrome (Orphanet:85278)
Cutis laxa (Orphanet:209)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Glycogen storage disease due to acid maltase deficiency, infantile onset (Orphanet:308552)
HYDROCEPHALUS, NORMAL-PRESSURE (OMIM:236690)
Hinman syndrome (Orphanet:84085)
Huntington disease-like 3 (Orphanet:157946)
Hyperkalemic periodic paralysis (Orphanet:682)
Infant botulism (Orphanet:178478)
Kleefstra syndrome (Orphanet:261494)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Ochoa syndrome (Orphanet:2704)
PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO (OMIM:176780)
Pelizaeus-Merzbacher disease (Orphanet:702)
Scleroderma (Orphanet:801)
Spastic paraplegia type 2 (Orphanet:99015)
Townes-Brocks syndrome (Orphanet:857)
Wolfram syndrome 1 (OMIM:222300)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)