Phenotypes for disease #03831 (CWS5 (Cowden syndrome, type 5 (CWS-5)), OMIM:615108)

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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     
0000343744 HP:0000750 Delayed speech and language development HP:0001270 Motor delay HP:0001300 Parkinsonism HP:0001250 Seizure NO signs of overgrowth Normal brain MRI Epileptic encephalopathy - Familial, autosomal dominant 30y - 03y Chilhood onset - Maria Elena García Paya 00455153
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