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.
Metachromatic leukodystrophy, adult type
Metachromatic leukodystrophy, congenital type
Metachromatic leukodystrophy, juvenile type
Metachromatic leukodystrophy, late infantile type
Deficiency of cerebroside-sulfatase
Severe deficiency of arylsulfatase
Delta cell tumor
Frequent (30-79%)
Metachromatic leukodystrophy
Quick Facts
- SNOMED CT
- 51047007
- UMLS CUI
- C0232769
- Fully Specified Name
- Abnormal gallbladder function (finding)
- Associated Conditions
- 8
- 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.