Phenotypes for disease #00284 (epilepsy, myoclonic, dystonia, hemiparesis, autonomic signs, lethargy, progressive diffuse cerebral atrophy)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000041532 epilepsy and ataxia cerebellar ataxia EA2 Familial, autosomal dominant - - 12y - - Erik-Jan Kamsteeg 00054868
0000324086 severe intellectual disability, spastic quadriplegia, epilepsy, facial abnormalities - - Unknown - - - - - Marketa Wayhelova 00433663
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