FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	gangliosidosis	ID (Ontology)	DOID:2368 (Human Disease)
Definition	A sphingolipidosis that is characterized by the accumulation of lipids known as gangliosides.
Comment
Links to External Ontologies
	DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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Spanning Tree (Parents/Children)

autosomal genetic disease
 |__autosomal recessive disease__
lipid storage disease            |
 |__sphingolipidosis_____________|
                                 gangliosidosis  5 rec.
                                  |__GM1 gangliosidosis 2 rec.
                                  |   |__GM1 gangliosidosis type 1 2 rec.
                                  |   |__GM1 gangliosidosis type 2 2 rec.
                                  |   |__GM1 gangliosidosis type 3 2 rec.
                                  |__GM2 gangliosidosis 3 rec.
                                      |__GM2 gangliosidosis, AB variant
                                      |__Sandhoff disease 3 rec.
                                      |__Tay-Sachs disease 3 rec.

Spanning Tree View Settings
Parents/Children View Depth	Show hierarchy levels: for parents, for children
Relationships
Is a	autosomal recessive disease sphingolipidosis
Part of
Synonyms & Secondary IDs
Synonyms

Secondary IDs

External Crossreferences & Linkouts
	GARD:12510 ICD10CM:E75.10 MESH:D005733 ORDO:309144 SNOMEDCT_US_2023_03_01:50967008 UMLS_CUI:C0017083