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ENPontocerebellar Hypoplasia, Type 17 (PCH17)
Alias:
Pch17
Hypoplasia, Pontocerebellar, Type 17
Pontocerebellar Hypoplasia, Iia 17
Pontocerebellar Hypoplasia 17
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Pontocerebellar Hypoplasia, Type 17, is also known as pch17. An important gene associated with Pontocerebellar Hypoplasia, Type 17 is PRDM13 (PR/SET Domain 13). Affiliated tissues include pons and cerebellum, and related phenotypes are global developmental delay and motor delay
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MALACARDS
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