juvenile neuronal ceroid lipofuscinosis
MONDO:0019262Mondo
Findings
No curated finding names juvenile neuronal ceroid lipofuscinosis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterized by onset at early school age with vision loss due to retinopathy, seizures and the decline of mental and motor capacities.
Definition from the Mondo Disease Ontology (MONDO:0019262), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (8)
- juvenile neuronal ceroid lipofuscinosis 1
- juvenile neuronal ceroid lipofuscinosis 10
- juvenile neuronal ceroid lipofuscinosis 2
- juvenile neuronal ceroid lipofuscinosis 3
- juvenile neuronal ceroid lipofuscinosis 5
- juvenile neuronal ceroid lipofuscinosis 6
- neuronal ceroid lipofuscinosis 9
- parkinsonism due to ATP13A2 deficiency
Other names
4 names
Resolves to: juvenile neuronal ceroid lipofuscinosis
- Also called
- batten diseaseJNCLjuvenile NCLSpielmeyer-Vogt disease