Phenotypes for disease #04586 (MRD39 (mental retardation, autosomal dominant, type 39 (MRD-39)), OMIM:616521)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000295673 Generalized-onset seizure, Seizure, Obesity, Intellectual disability, severe, Intellectual disability - - Isolated (sporadic) 21y - - - - Andreas Laner 00402925
0000300100 Delayed speech and language development, Behavioral abnormality, Global developmental delay, Neurodevelopmental delay, Urinary incontinence, Low frustration tolerance, Short attention span, Tip-toe gait - - Isolated (sporadic) 03y - - - - Andreas Laner 00407970
0000350793 Hypotonia, Delayed speech and language development, Microcephaly - - Unknown 04y - - - - Andreas Laner 00465255
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