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MIM:610297 - PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO; PARK13
Xenbase Genes: htra2
Human Disease Resource: MIM
MONDO:0012466 - extraembryonic cavity |
MONDO:0017279 - young-onset Parkinson disease |
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MONDO:0012466 - extraembryonic cavity |
MONDO:0017279 - young-onset Parkinson disease |