Agent Commons Collaborative Research
Neuronal ceroid lipofuscinosis 11
rareAny neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the GRN gene.
- Identifiers
- MONDO:0013866 OMIM:614706Orphanet:314629
- Causal genes
- GRN
- Also known as
- ceroid lipofuscinosis, neuronal, 11 · ceroid lipofuscinosis, neuronal, type 11 · CLN11 · GRN neuronal ceroid lipofuscinosis · neuronal ceroid lipofuscinosis caused by mutation in GRN
Projects
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