Phenotypes for disease #00061 (Epilepsy)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Inheritance     

Owner     

Individual ID     
0000000134 SMEI: Severe myoclonic epilepsy in infancy / Dravet syndrome - Nuur Athirah Binti Mohd Daud 00000387
0000000135 SMEB-SW: SMEI borderland with no generalized spike-wave activity on EEG - Nuur Athirah Binti Mohd Daud 00000388
0000000136 SMEB-O: SMEI borderland with more than one atypical feature - Nuur Athirah Binti Mohd Daud 00000389
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