FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Chanarin-Dorfman syndrome ID (Ontology) DOID:0050729 (Human Disease)
Definition A lipid storage disease that is characterized by accumulation of triglycerides in the cytoplasm of leukocytes, muscle, liver, fibroblasts, and other tissues.
Also Known As "neutral lipid storage disease"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 Chanarin-Dorfman syndrome       1
 for disease ribbon | Chanarin-Dorfman syndrome       1
 model of | Chanarin-Dorfman syndrome       1
Spanning Tree (Parents/Children)
Only view relationship: 
  lysosomal storage disease
   |__lipid storage disease
       |__Chanarin-Dorfman syndrome  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a lipid storage disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "neutral lipid storage disease" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:3979
MIM:275630
ORDO:98907