ICD-10-CM Alphabetic Index to Diseases and Injuries
Disability, disabilities
Follow the subterms below to reach a more specific code.ICD-10 code for Disability — guide and common questions →
- heart — see Disease, heart
- intellectual F79
- with
- autistic features F84.9
- pathogenic CHAMP1 (genetic) (variant) F78.A9
- pathogenic HNRNPH2 (genetic) (variant) F78.A9
- pathogenic SATB2 (genetic) (variant) F78.A9
- pathogenic SETBP1 (genetic) (variant) F78.A9
- pathogenic STXBP1 (genetic) (variant) F78.A9
- pathogenic SYNGAP1 (genetic) (variant) F78.A1
- autosomal dominant F78.A9
- autosomal recessive F78.A9
- genetic related F78.A9
- with
- pathogenic CHAMP1 (variant) F78.A9
- pathogenic HNRNPH2 (variant) F78.A9
- pathogenic SATB2 (variant) F78.A9
- pathogenic SETBP1 (variant) F78.A9
- pathogenic STXBP1 (variant) F78.A9
- pathogenic SYNGAP1 (variant) F78.A1
- specified NEC F78.A9
- SYNGAP1-related F78.A1
- in
- autosomal dominant mental retardation F78.A9
- autosomal recessive mental retardation F78.A9
- SATB2-associated syndrome F78.A9
- SETBP1 disorder F78.A9
- STXBP1 encephalopathy with epilepsy F78.A9 — see also Encephalopathy; and see also Epilepsy
- X-linked mental retardation (syndromic) (Bain type) F78.A9
- mild (I.Q.50-69) F70
- moderate (I.Q.35-49) F71
- profound (I.Q. under 20) F73
- severe (I.Q.20-34) F72
- specified level NEC F78.A9
- SYNGAP1-related F78.A1
- X-linked (syndromic) (Bain type) F78.A9
- knowledge acquisition F81.9
- learning F81.9
- limiting activities Z73.6
- spelling, specific F81.81