Phenotype #0000000134

Individual ID 00000387
Associated disease -
Phenotype details SMEI: Severe myoclonic epilepsy in infancy / Dravet syndrome
Inheritance -
Owner name Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud

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