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neuronal ceroid lipofuscinosis 11 | RareConnect | RareConnect.io

/adult neuronal ceroid lipofuscinosis

/neuronal ceroid lipofuscinosis 11

neuronal ceroid lipofuscinosis 11

Rare Disease

MONDO:0013866

Also Known As

CLN11GRN neuronal ceroid lipofuscinosisGrn neuronal ceroid lipofuscinosisceroid lipofuscinosis, neuronal, type 11neuronal ceroid lipofuscinosis caused by mutation in GRNneuronal ceroid lipofuscinosis caused by mutation in Grnneuronal ceroid lipofuscinosis type 11CLN11 diseaseceroid lipofuscinosis, neuronal, 11

Definition

Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the GRN 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:614706 ↗

Orphanet

Orphanet:314629 ↗

GARD

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