ICD-10-CM Disability, disabilities References

"Disability, disabilities" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries

Browse the ICD-10-CM codes with references applicable to the clinical term "disability, disabilities"

• Disability, disabilities
  • heart - See: Disease, heart;
  • intellectual - F79 Unspecified intellectual disabilities
    • autosomal dominant - F78.A9 Other genetic related intellectual disability
    • autosomal recessive - F78.A9 Other genetic related intellectual disability
    • genetic related - F78.A9 Other genetic related intellectual disability
      • specified NEC - F78.A9 Other genetic related intellectual disability
      • SYNGAP1-related - F78.A1 SYNGAP1-related intellectual disability
      • with
        • pathogenic CHAMP1 (variant) - F78.A9 Other genetic related intellectual disability
        • pathogenic HNRNPH2 (variant) - F78.A9 Other genetic related intellectual disability
        • pathogenic SATB2 (variant) - F78.A9 Other genetic related intellectual disability
        • pathogenic SETBP1 (variant) - F78.A9 Other genetic related intellectual disability
        • pathogenic STXBP1 (variant) - F78.A9 Other genetic related intellectual disability
        • pathogenic SYNGAP1 (variant) - F78.A1 SYNGAP1-related intellectual disability
    • in
      • autosomal dominant mental retardation - F78.A9 Other genetic related intellectual disability
      • autosomal recessive mental retardation - F78.A9 Other genetic related intellectual disability
      • SATB2-associated syndrome - F78.A9 Other genetic related intellectual disability
      • SETBP1 disorder - F78.A9 Other genetic related intellectual disability
      • STXBP1 encephalopathy with epilepsy - See Also: Encephalopathy; and see also Epilepsy; - F78.A9 Other genetic related intellectual disability
      • X-linked mental retardation (syndromic) (Bain type) - F78.A9 Other genetic related intellectual disability
    • mild (I.Q.50-69) - F70 Mild intellectual disabilities
    • moderate (I.Q.35-49) - F71 Moderate intellectual disabilities
    • profound (I.Q. under 20) - F73 Profound intellectual disabilities
    • severe (I.Q.20-34) - F72 Severe intellectual disabilities
    • specified level NEC - F78.A9 Other genetic related intellectual disability
    • SYNGAP1-related - F78.A1 SYNGAP1-related intellectual disability
    • with
      • autistic features - F84.9 Pervasive developmental disorder, unspecified
      • pathogenic CHAMP1 (genetic) (variant) - F78.A9 Other genetic related intellectual disability
      • pathogenic HNRNPH2 (genetic) (variant) - F78.A9 Other genetic related intellectual disability
      • pathogenic SATB2 (genetic) (variant) - F78.A9 Other genetic related intellectual disability
      • pathogenic SETBP1 (genetic) (variant) - F78.A9 Other genetic related intellectual disability
      • pathogenic STXBP1 (genetic) (variant) - F78.A9 Other genetic related intellectual disability
      • pathogenic SYNGAP1 (genetic) (variant) - F78.A1 SYNGAP1-related intellectual disability
    • X-linked (syndromic) (Bain type) - F78.A9 Other genetic related intellectual disability
  • knowledge acquisition - F81.9 Developmental disorder of scholastic skills, unspecified
  • learning - F81.9 Developmental disorder of scholastic skills, unspecified
  • limiting activities - Z73.6 Limitation of activities due to disability
  • spelling, specific - F81.81 Disorder of written expression