Neuronal ceroid lipofuscinosis 13

Definition

Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the CTSF gene.

Also known as ceroid lipofuscinosis, neuronal, 13 (Kufs type), ceroid lipofuscinosis, neuronal, type 13, CLN13, CTSF neuronal ceroid lipofuscinosis, neuronal ceroid lipofuscinosis caused by mutation in CTSF, neuronal ceroid lipofuscinosis type 13 — per MONDO

Also identified as

• DOID 0110727 per MONDO
• OMIM 615362 per MONDO
• Orphanet 352709 per MONDO
• UMLS C3715049 per MONDO