Global Variome shared LOVD

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Phenotype #0000157091 Individual ID 00208268 Associated disease migraine Diagnosis/Initial familial hemiplegic migraine Diagnosis/Definite - Phenotype details 1st HMA no language disturbances, 1st HMA no sensory disturbances, 1st HMA no visual disturbances, 1st HMA confusion/somnolence; 1st severe attack signs mild coma/fever; PermCer status, no nystagmus, dysarthria, no ataxia, Cerebral MRI cerebral cortical atrophy Inheritance Familial Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name LOVD Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2008-06-18 23:00:08 +02:00 (CEST) Date last edited 2008-06-18 23:00:08 +02:00 (CEST)

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