Phenotypes for disease #06356 (MRD57 (Mental retardation, autosomal dominant 57), OMIM:618050)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000340329 - - Neurodevelopmental delay, Hypotonia, Microcephaly, Gait disturbance, Joint hypermobility, Constipation, Hyperactivity, Tip-toe gait Unknown 01y - - - Andreas Laner 00451668
0000346198 - - Microcephaly, Autism, Intellectual disability, Developmental regression, EEG abnormality, Short stature, Decreased body weight, Upslanted palpebral fissure, Long nose, Abnormality of the outer ear Isolated (sporadic) 10y - - - Andreas Laner 00457749
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