Phenotypes for disease #00821 (MRXSH (mental retardation, X-linked, syndromic, Hedera type (MRXSH)), OMIM:300423)

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AscendingPhenotype ID     

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Individual ID     
0000105559 see paper; ..., X-linked mental retardation, epilepsy - - Familial, X-linked recessive - - - seizures, ataxia - - Johan den Dunnen 00132794
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