has material basis in germline mutation in GRIN1 neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant https://github.com/monarch-initiative/mondo/issues/9063 https://www.malacards.org/card/autosomal_dominant_intellectual_developmental_disorder_8 https://www.malacards.org/card/neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures_autosomal_dominant MONDO:0013655 NDHMSD intellectual disability, autosomal dominant 8 UMLS:C3280282 Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIN1 gene. MRD8 mental retardation, autosomal dominant 8, formerly MEDGEN:481912 autosomal dominant intellectual disability 8 mental retardation, autosomal dominant 8 DOID:0070038 intellectual disability, autosomal dominant type 8 GARD:0013686 GRIN1 autosomal dominant non-syndromic intellectual disability mental retardation, autosomal dominant type 8 neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1 OMIM:614254 intellectual disability, autosomal dominant GRIN1-related complex neurodevelopmental disorder