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Reference

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A reference for what the literature reports. Not medical advice.

Disease

infantile neuronal ceroid lipofuscinosis

MONDO:0019261Mondo

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Findings

No curated finding names infantile neuronal ceroid lipofuscinosis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

A form of neuronal ceroid lipofuscinosis (NCL) characterized by onset during the second half of the first year of life and rapid mental and motor deterioration leading to loss of all psychomotor abilities.

Definition from the Mondo Disease Ontology (MONDO:0019261), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: cerebral lipidosis with dementia
neuronal ceroid lipofuscinosis
Narrower terms (2): infantile neuronal ceroid lipofuscinosis 1
infantile neuronal ceroid lipofuscinosis 2

Other names

6 names

Resolves to: infantile neuronal ceroid lipofuscinosis

Also called: Classic Infantile CLN1 DiseaseHagberg-Santavuori diseaseINCLinfantile NCLSantavuori diseaseSantavuori-Haltia disease