Abdominal distention

Symptom Information:

Symptom ID: HPO:0003270
Synonyms:
Abdominal distension [HPO:0003270]
Abdominal swelling [HPO:0003270]
Distended abdomen [HPO:0003270]
Abdominal distention [OMIM:Abdominal distention]
Distended abdomen [OMIM:Distended abdomen]
Abdominal distention (children) [OMIM:Abdominal distention (children)]
Abdominal distension [MedDRA:10000060]
Quality:
Cross references:
OMIM: "Abdominal distention" [OMIM:Abdominal distention]
OMIM: "Distended abdomen" [OMIM:Distended abdomen]
OMIM: "Abdominal distention (children)" [OMIM:Abdominal distention (children)]
Is a (Direct Parents):
MedDRA Flatulence, bloating and distension
HPO         Abdominal symptom
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abdominal symptom(HPO:0011458)
             Abdominal distention(HPO:0003270)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Gastrointestinal signs and symptoms(MedDRA:10018012)
       Flatulence, bloating and distension(MedDRA:10016770)
          Abdominal distention(HPO:0003270)
Database Frequency: 46 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins (Orphanet:217371)
Alström syndrome (Orphanet:64)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Colonic atresia (Orphanet:1198)
Congenital chloride diarrhea (Orphanet:53689)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Congenital short bowel syndrome (Orphanet:2301)
Congenital sodium diarrhea (Orphanet:103908)
Currarino triad (Orphanet:1552)
ENTEROCOLITIS (OMIM:226150)
Early-onset familial noncirrhotic portal hypertension (ORPHA:494348)
Fabry disease (Orphanet:324)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 3 (Orphanet:77261)
Glucose-galactose malabsorption (Orphanet:35710)
Glycogen storage disease due to GLUT2 deficiency (Orphanet:2088)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:142623)
Hemochromatosis, type 2A (OMIM:602390)
Hirschsprung disease (Orphanet:388)
Hypochondrogenesis (Orphanet:93297)
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED (OMIM:300048)
Idiopathic copper-associated cirrhosis (Orphanet:209919)
Isolated polycystic liver disease (Orphanet:2924)
Leprechaunism (Orphanet:508)
Letterer-Siwe disease (Orphanet:99870)
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) (OMIM:613662)
Meckel syndrome, type 8 (OMIM:613885)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (Orphanet:2241)
Mowat-Wilson syndrome (Orphanet:2152)
Mulibrey nanism (Orphanet:2576)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Neonatal hemochromatosis (Orphanet:446)
Oculogastrointestinal muscular dystrophy (Orphanet:1876)
Primary Fanconi syndrome (Orphanet:3337)
Qazi-Markouizos syndrome (Orphanet:3010)
Reticular dysgenesis (Orphanet:33355)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Thyroid ectopia (Orphanet:95712)
Thyroid hemiagenesis (Orphanet:95719)