Phenotypes for disease #00795 (MRD5 (mental retardation, autosomal dominant, type 5 (MRD-5)), OMIM:612621)

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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     
0000351241 Neurodevelopmental delay, Esophageal atresia, Short stature, Decreased body weight, Very preterm birth - - Isolated (sporadic) 13y - - - - - Andreas Laner 00465799
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