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neuronal ceroid lipofuscinosis 13 | RareConnect | RareConnect.io

/adult neuronal ceroid lipofuscinosis

/neuronal ceroid lipofuscinosis 13

neuronal ceroid lipofuscinosis 13

Rare Disease

MONDO:0014147

Also Known As

CLN13CTSF neuronal ceroid lipofuscinosisceroid lipofuscinosis, neuronal, 13 (Kufs type)ceroid lipofuscinosis, neuronal, type 13neuronal ceroid lipofuscinosis 13 Kufs typeneuronal ceroid lipofuscinosis caused by mutation in CTSFneuronal ceroid lipofuscinosis type 13CLN13 diseaseceroid lipofuscinosis, neuronal, 13ceroid lipofuscinosis, neuronal, 13, Kufs type

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615362 ↗

Orphanet

Orphanet:352709 ↗

GARD

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