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

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     
0000285078 Myoclonus, Absent speech, Atypical absence seizure, Multifocal epileptiform discharges, Severe global developmental delay - - Familial, X-linked dominant 05y - - - - - Andreas Laner 00391755
0000337075 Intellectual disability, mild, Receptive language delay, Heterophoria - - Unknown 13y - - - - - Andreas Laner 00447881
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