F78.A9✓ Billable

Other genetic related intellectual disability

Also Indexed As(ICD-10-CM Alphabetic Index)

These clinical terms, synonyms, and manifestations all map to F78.A9 in the official ICD-10-CM Alphabetic Index.

Disability, disabilities, intellectual, X-linked (syndromic) (Bain type)Disability, disabilities, intellectual, autosomal dominantDisability, disabilities, intellectual, autosomal recessiveDisability, disabilities, intellectual, genetic relatedDisability, disabilities, intellectual, genetic related, specified NECDisability, disabilities, intellectual, genetic related, with, pathogenic CHAMP1 (variant)Disability, disabilities, intellectual, genetic related, with, pathogenic HNRNPH2 (variant)Disability, disabilities, intellectual, genetic related, with, pathogenic SATB2 (variant)Disability, disabilities, intellectual, genetic related, with, pathogenic SETBP1 (variant)Disability, disabilities, intellectual, genetic related, with, pathogenic STXBP1 (variant)Disability, disabilities, intellectual, in, SATB2-associated syndromeDisability, disabilities, intellectual, in, SETBP1 disorderDisability, disabilities, intellectual, in, STXBP1 encephalopathy with epilepsyDisability, disabilities, intellectual, in, X-linked mental retardation (syndromic) (Bain type)Disability, disabilities, intellectual, in, autosomal dominant mental retardationDisability, disabilities, intellectual, in, autosomal recessive mental retardationDisability, disabilities, intellectual, specified level NECDisability, disabilities, intellectual, with, pathogenic CHAMP1 (genetic) (variant)Disability, disabilities, intellectual, with, pathogenic HNRNPH2 (genetic) (variant)Disability, disabilities, intellectual, with, pathogenic SATB2 (genetic) (variant)Disability, disabilities, intellectual, with, pathogenic SETBP1 (genetic) (variant)Disability, disabilities, intellectual, with, pathogenic STXBP1 (genetic) (variant)

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