Phenotypes for disease #00342 (LISX1;SCLH (lissencephaly, X-linked, type 1 (subcortical laminar heterotopia (SCLH))), OMIM:300067)

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AscendingPhenotype ID     

Phenotype details     

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Age/Examination     

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Owner     

Individual ID     
0000014922 diagnosis subcortical laminar heterotopia, X-linked, included - - Unknown - - - - - Lab Zuffardi 00016317
0000274789 Double-Cortex syndrome with Seizure, Motor seizure, Myoclonic seizure - 28y Familial, X-linked - - - - - Andreas Laner 00380936
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