Bowel incontinence
Symptom Information:
Symptom ID: | HPO:0002607 | |||||||||||||
Synonyms: |
|
|||||||||||||
Quality: | ||||||||||||||
Cross references: |
|
|||||||||||||
Is a (Direct Parents): |
|
|||||||||||||
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) |