Phenotypes for disease #01118 (XLID9;MRX9 (intellectual developmental disorder, X-linked, type 9), OMIM:309549)

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AscendingPhenotype ID     

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Individual ID     
0000280738 Neurodevelopmental delay, Muscular hypotonia, Dystonia, Foot dorsiflexor weakness, Abnormal putamen morphology, Abnormality of the cerebral white matter, Hydrocephalus, Abnormality of the midface - - Unknown 01y - - - - Andreas Laner 00386941
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