Disability, disabilities is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). It has 40 subterms and 36 code entries. First-level subterms include heart, intellectual, knowledge acquisition, learning, limiting activities, spelling, specific. Confirm any code you find here in the Tabular List before you report it.
Subterms 40 Expand all Collapse all
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 see also Encephalopathy; and see also Epilepsy F78.A9 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