Phenotypes for disease #05841 (glycine encephalopathy (encephalopathy, glycine, with normal serum glycine), OMIM:617301)

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AscendingPhenotype ID     

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Individual ID     
0000237057 arthrogryposis and severe neurological impairment GLYT1 encephalopathy neonatal onset, respiratory failure, severe hypotonia at birth that progressed to limb hypertonicity, absent neonatal reflexes, startle-like responses provoked by sudden loud sounds and tactile stimulation, severe global developmental delay, dysmorphic features, arthrogryposis multiplex congenita Familial, autosomal recessive - - - - Irene Mademont Soler 00311052
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