Phenotypes for disease #00792 (MRD1 (mental retardation, autosomal dominant, type 1 (MRD-1)), OMIM:156200)

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     

Birth_Details     

Protein     

Owner     

Individual ID     
0000060538 Mental retardation, autosomal dominant 1 (OMIM:156200) - - Isolated (sporadic) - - - - - - Daniel Trujillano 00080969
0000258102 Seizure, Encephalopathy - - Unknown 01y - - - - - Andreas Laner 00362732
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