Phenotypes for disease #00009 (EPM1A (epilepsy, myoclonic, progressive, type 1A (EPM1A, Unverricht and Lundborg)), OMIM:254800)

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

Phenotype details     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000002023 lissencephaly, ambiguous genitalia, agenesis corpus callosum - Isolated (sporadic) - - - - - - Johan den Dunnen 00003183
0000002095 - - Isolated (sporadic) - - - - - - Johan den Dunnen 00003256
0000070612 neurodegenerative phenotype, neurotransmitter abnormalities; seizures responded to Levocarbidopa and 5OH-tryptophan - Familial, autosomal recessive - - - - - - Johan den Dunnen 00092276
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