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late infantile neuronal ceroid lipofuscinosis
Disease Summary
Associated Targets (15)
Tbio
9
Tchem
4
Tclin
2
Mondo Description Late infantile neuronal ceroid lipofuscinoses (LINCLs) are 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.
Mondo Term and Equivalent IDs
MONDO:0015674: late infantile neuronal ceroid lipofuscinosis
Download Data for late infantile neuronal ceroid lipofuscinosis
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:168491
SCTID:14637005
MONDO:0015674
High level summary of knowledge for a disease, including descriptions and datasource references.