Disability, disabilities - in the ICD-10-CM Index
Annotation Back-References in the 2025 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.
