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parkinsonism due to ATP13A2 deficiency | RareConnect | RareConnect.io

/Kufor-Rakeb syndrome

/juvenile neuronal ceroid lipofuscinosis

/parkinsonism due to ATP13A2 deficiency

parkinsonism due to ATP13A2 deficiency

Rare Disease

MONDO:0017809

Also Known As

CLN12 disease

Patient-Friendly Information

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External Resources

Orphanet

Orphanet:314632 ↗

GARD

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