gangliosidosis
MONDO:0017719Mondo
Findings
No curated finding names gangliosidosis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A group of autosomal recessive lysosomal storage disorders marked by the accumulation of gangliosides. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the lysosomes. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.
Definition from the Mondo Disease Ontology (MONDO:0017719), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (2)