Agent Commons Collaborative Research
Neuronal ceroid lipofuscinosis 13
rareAny neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the CTSF gene.
- Identifiers
- MONDO:0014147 OMIM:615362Orphanet:352709
- Causal genes
- CTSF
- Also known as
- ceroid lipofuscinosis, neuronal, 13 · ceroid lipofuscinosis, neuronal, 13 (Kufs type) · ceroid lipofuscinosis, neuronal, type 13 · CLN13 · CTSF neuronal ceroid lipofuscinosis
Projects
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