Gastrointestinal dysmotility

Symptom Information:

Symptom ID: HPO:0002579
Synonyms:
Gastrointestinal dysmotility [OMIM:Gastrointestinal dysmotility]
Gastrointestinal dysmotility (CVS+) [OMIM:Gastrointestinal dysmotility (CVS+)]
Quality:
Cross references:
OMIM: "Gastrointestinal dysmotility" [OMIM:Gastrointestinal dysmotility]
OMIM: "Gastrointestinal dysmotility (CVS+)" [OMIM:Gastrointestinal dysmotility (CVS+)]
Is a (Direct Parents):
HPO         Abnormality of the gastrointestinal tract
HPO         Small intestinal dysmotility
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)
                Gastrointestinal dysmotility(HPO:0002579)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Alpers syndrome (Orphanet:726)
Behr syndrome (Orphanet:1239)
CYCLIC VOMITING SYNDROME (OMIM:500007)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Fabry disease (Orphanet:324)
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) (OMIM:603041)
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) (OMIM:613662)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (Orphanet:2241)
Mitochondrial neurogastrointestinal encephalomyopathy (Orphanet:298)
Posterior column ataxia - retinitis pigmentosa (Orphanet:88628)
Smith-Lemli-Opitz syndrome (Orphanet:818)