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
- 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.
