Phenotypes for disease #05861 (NEDSWMA;CPSQ1 (neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (CPSQ1)), OMIM:619026)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

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Individual ID     
0000268810 - Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (OMIM 618994) HP:0002353; HP:0002539; HP:0002079; HP:0003155; HP:0012704; HP:0001263; HP:0001250; HP:0001276 Familial, autosomal recessive - - - - Wenjuan Qiu 00373536
0000269010 - Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (OMIM 618994) HP:0002353; HP:0002539; HP:0002079; HP:0003155; HP:0012704; HP:0001263; HP:0001250; HP:0001276 Familial, autosomal recessive - - - - Wenjuan Qiu 00373800
0000276846 Spastic paraplegia Ataxia - Familial, autosomal recessive 11y 11y 00y - Baiba Lace 00383056
0000328186 - - Intellectual disability, Heterotropia, Seizure, Secondary microcephaly Isolated (sporadic) 15y - - - Andreas Laner 00438282
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