Phenotypes for disease #01066 (MRXSSD (mental retardation syndrome, X-linked, Siderius type (MRXSSD)), OMIM:300263)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     

Individual ID     
0000323918 Neurodevelopmental delay, Focal-onset seizure, Obesity, Polyphagia - - Isolated (sporadic) 08y - - - - - Andreas Laner 00433442
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