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paternal 14q32.2 hypomethylation syndrome | RareConnect | RareConnect.io

/motor developmental delay due to 14q32.2 paternally expressed gene defect

/paternal 14q32.2 hypomethylation syndrome

paternal 14q32.2 hypomethylation syndrome

Rare Disease

MONDO:0016782

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Orphanet

Orphanet:254531 ↗

GARD

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