Abdominal distention
Symptom Information:
Symptom ID: | HPO:0003270 | |||||||
Synonyms: |
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Cross references: |
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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) |
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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) |