heart, see [Disease, heart]

intellectualF79

with

autistic featuresF84.9

pathogenic CHAMP1 F78.A9

pathogenic HNRNPH2 F78.A9

pathogenic SATB2 F78.A9

pathogenic SETBP1 F78.A9

pathogenic STXBP1 F78.A9

pathogenic SYNGAP1 F78.A1

autosomal dominantF78.A9

autosomal recessiveF78.A9

genetic relatedF78.A9

with

pathogenic CHAMP1 (variant)F78.A9

pathogenic HNRNPH2 (variant)F78.A9

pathogenic SATB2 (variant)F78.A9

pathogenic SETBP1 (variant)F78.A9

pathogenic STXBP1 (variant)F78.A9

pathogenic SYNGAP1 (variant)F78.A1

specified NECF78.A9

SYNGAP1-relatedF78.A1

in

autosomal dominant mental retardationF78.A9

autosomal recessive mental retardationF78.A9

SATB2-associated syndromeF78.A9

SETBP1 disorderF78.A9

STXBP1 encephalopathy with epilepsy, see also [Encephalopathy; and see also Epilepsy]F78.A9

X-linked mental retardation F78.A9

mild F70

moderate F71

profound F73

severe F72

specified level NECF78.A9

SYNGAP1-relatedF78.A1

X-linked F78.A9

knowledge acquisitionF81.9

learningF81.9

limiting activitiesZ73.6

spelling, specificF81.81