Phenotypes for disease #00851 (SHMS;MRD17 (Schuurs-Hoeijmakers syndrome (SHMS, mental retardation, autosomal dominant, type 17 (MRD-17))), OMIM:615009)

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AscendingPhenotype ID     

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Individual ID     
0000070578 severe IDD, microcephaly, facial dysmorphisms, myopia, bifid uvula and submucous cleft, dysplastic pulmonary, aortic valves, failure to thrive progressive ataxia and cerebellar atrophy; neurodegeneration progressive cerebellar atrophy - - Familial, autosomal dominant - - - - - - Johan den Dunnen 00092244
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