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MIM:212840 - GORDON HOLMES SYNDROME; GDHS
Xenbase Genes: rnf216
Human Disease Resource: MIM
MONDO:0008935 - cerebellar ataxia-hypogonadism syndrome |
DOID:0111587 - Gordon Holmes syndrome |
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MONDO:0008935 - cerebellar ataxia-hypogonadism syndrome |
DOID:0111587 - Gordon Holmes syndrome |