Phenotypes for disease #03661 (BSVD2;POREN2 (brain small vessel disease, type 2 (BSVD2);porencephaly type 2 (POREN2)), OMIM:614483)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Owner     

Individual ID     
0000258876 Dystonic movement disorder, severe generalised dystonia, scoliosis, epilepsy (myoclonic), porencephaly, cognition less affected than motor function, no speech, no voluntary motor function, sister with mild porencephaly - - Unknown - 12y - - - Andreas Laner 00363527
0000337724 Cerebral palsy, Hemiparesis, Periventricular leukomalacia, Ventriculomegaly, Esodeviation, Delayed speech and language development, Delayed gross motor development, EEG with focal sharp waves, Abnormality of refraction, Symptomatic seizures - - Unknown 02y - - - - Andreas Laner 00448541
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