Phenotypes for disease #00822 (MRX1 (mental retardation, X-linked, type 1), OMIM:309530)

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     

Individual ID     
0000285078 Myoclonus, Absent speech, Atypical absence seizure, Multifocal epileptiform discharges, Severe global developmental delay - - Familial, X-linked dominant 05y - - - - - Andreas Laner 00391755
Legend   How to query