Disability, disabilities

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

References in the ICD-10-CM Index to Diseases and Injuries 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
      • 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
      • 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

Applicable Clinical Terms Definitions

Heart: The hollow, muscular organ that maintains the circulation of the blood.

Learning: Relatively permanent change in behavior that is the result of past experience or practice. The concept includes the acquisition of knowledge.