Index to Diseases and Injuries

Disability, disabilities

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

Use the index to find a code, then confirm it in the Tabular List before assigning it. A code ending in a dash is incomplete, and a code in [brackets] is a manifestation code reported after the underlying condition. Search the whole index.

ICD-10-CM Index to Diseases and Injuries maintained by CDC/NCHS (public domain), from the CMS FY2027 release.