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myoclonus, familial, 1 | RareConnect | RareConnect.io

/myoclonus, familial

/myoclonus, familial, 1

myoclonus, familial, 1

Rare Disease

MONDO:0100093

Also Known As

myoclonus, familial corticalFCMMYOCL1

Definition

Familial cortical myoclonus caused by heterozygous mutation in the NOL3 gene on chromosome 16q22.

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:614937 ↗

Related Diseases

myoclonus, familial, 2

MONDO:0100092

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