Disability, disabilities
- heartSee Disease, heart
- intellectualF79
- intellectual, with
- intellectual, with, autistic featuresF84.9
- intellectual, with, pathogenic CHAMP1 (genetic) (variant)F78.A9
- intellectual, with, pathogenic HNRNPH2 (genetic) (variant)F78.A9
- intellectual, with, pathogenic SATB2 (genetic) (variant)F78.A9
- intellectual, with, pathogenic SETBP1 (genetic) (variant)F78.A9
- intellectual, with, pathogenic STXBP1 (genetic) (variant)F78.A9
- intellectual, with, pathogenic SYNGAP1 (genetic) (variant)F78.A1
- intellectual, autosomal dominantF78.A9
- intellectual, autosomal recessiveF78.A9
- intellectual, genetic relatedF78.A9
- intellectual, genetic related, with
- intellectual, genetic related, with, pathogenic CHAMP1 (variant)F78.A9
- intellectual, genetic related, with, pathogenic HNRNPH2 (variant)F78.A9
- intellectual, genetic related, with, pathogenic SATB2 (variant)F78.A9
- intellectual, genetic related, with, pathogenic SETBP1 (variant)F78.A9
- intellectual, genetic related, with, pathogenic STXBP1 (variant)F78.A9
- intellectual, genetic related, with, pathogenic SYNGAP1 (variant)F78.A1
- intellectual, genetic related, specified NECF78.A9
- intellectual, genetic related, SYNGAP1-relatedF78.A1
- intellectual, in
- intellectual, in, autosomal dominant mental retardationF78.A9
- intellectual, in, autosomal recessive mental retardationF78.A9
- intellectual, in, SATB2-associated syndromeF78.A9
- intellectual, in, SETBP1 disorderF78.A9
- intellectual, in, STXBP1 encephalopathy with epilepsyF78.A9
- intellectual, in, X-linked mental retardation (syndromic) (Bain type)F78.A9
- intellectual, mild (I.Q.50-69)F70
- intellectual, moderate (I.Q.35-49)F71
- intellectual, profound (I.Q. under 20)F73
- intellectual, severe (I.Q.20-34)F72
- intellectual, specified level NECF78.A9
- intellectual, SYNGAP1-relatedF78.A1
- intellectual, X-linked (syndromic) (Bain type)F78.A9
- knowledge acquisitionF81.9
- learningF81.9
- limiting activitiesZ73.6
- spelling, specificF81.81