has material basis in germline mutation in GRIA3 syndromic X-linked intellectual disability 94 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/7693 https://www.malacards.org/card/intellectual_developmental_disorder_x_linked_syndromic_wu_type https://www.malacards.org/card/syndromic_x_linked_intellectual_disability_94 syndromic X-linked intellectual disability Wu type A syndromic X-linked intellectual disability characterized by moderate intellectual disability with variable occurrence of asthenic body habitus, dysmorphic features, autistic features, macrocephaly, seizures, myoclonic jerks, and hyporeflexia that has material basis in mutation in the GRIA3 gene on chromosome Xq25. MRXS29 MEDGEN:437111 OMIM:300699 intellectual developmental disorder, X-linked, syndromic, Wu type, X-linked recessive Orphanet:364028 MESH:C567479 intellectual disability, X-linked, syndromic, Wu type MRX94 syndromic X-linked intellectual disability 29 GARD:0027794 MRXSW MONDO:0010402 DOID:0060823 intellectual disability, X-linked 94 mental retardation, X-linked, syndromic, Wu type syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 94 UMLS:C2678051 intellectual disability, X-linked, syndromic 29 mental retardation, X-linked, syndromic 29 mental retardation, X-linked 94 X-linked syndromic intellectual disability