late infantile neuronal ceroid lipofuscinosis
MONDO:0015674Mondo
Findings
No curated finding names late infantile 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 during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration.
Definition from the Mondo Disease Ontology (MONDO:0015674), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
4 names
Resolves to: late infantile neuronal ceroid lipofuscinosis
- Also called
- Jansky-Bielschowsky diseaselate infantile NCLlate-infantile neuronal ceroid lipofuscinosisLINCL