Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Biliary cirrhosis
Occasional (5-29%)
Mirizzi's syndrome
Occasional (5-29%)
Indian childhood cirrhosis
Insulin receptor defect
Frequent (30-79%)
Achondrogenesis, type IB
Hereditary fructosuria
Occasional (5-29%)
AL amyloidosis
Occasional (5-29%)
Metachromatic leukodystrophy, adult type
Occasional (5-29%)
Congenital secretory diarrhea, chloride type
Glycogen storage disease, type VI
Occasional (5-29%)
Congenital malrotation of intestine
Primary biliary cirrhosis
Occasional (5-29%)
Congenital atresia of colon
Occasional (5-29%)
Metachromatic leukodystrophy, congenital type
Occasional (5-29%)
Achondrogenesis, type IA
Very frequent (80-99%)
Smith-Lemli-Opitz syndrome
Always present (100%)
Metachromatic leukodystrophy, juvenile type
Occasional (5-29%)
Metachromatic leukodystrophy, late infantile type
Occasional (5-29%)
Congenital atresia of duodenum
Occasional (5-29%)
Hereditary spherocytosis
Very rare (1-4%)
Jarcho-Levin syndrome
Glycogenosis with glucoaminophosphaturia
Frequent (30-79%)
Multiple endocrine neoplasia, type 2
Occasional (5-29%)
Infantile nephropathic cystinosis
Frequent (30-79%)
Hereditary hollow viscus myopathy
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 41931001
- UMLS CUI
- C5980104
- Fully Specified Name
- Distension of abdomen (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.