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neuronal ceroid lipofuscinosis 8 | RareConnect | RareConnect.io

/late infantile neuronal ceroid lipofuscinosis

/juvenile neuronal ceroid lipofuscinosis

/neuronal ceroid lipofuscinosis 8

neuronal ceroid lipofuscinosis 8

Rare Disease

MONDO:0010830

Also Known As

CLN8CLN8 neuronal ceroid lipofuscinosisceroid lipofuscinosis, neuronal, type 8neuronal ceroid lipofuscinosis 8neuronal ceroid lipofuscinosis caused by mutation in CLN8neuronal ceroid lipofuscinosis type 8CLN8 diseaseceroid lipofuscinosis, neuronal, 8

Definition

Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the CLN8 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:600143 ↗

Orphanet

Orphanet:228354 ↗

GARD

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