Q74.3 Arthrogryposis multiplex congenitaBillable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis. Exempt from present-on-admission (POA) reporting.
Defines the logic of DRG(s) 564-566 in MDC 08.
754.89 Other specified nonteratogenic anomalies (approximate)G71 Primary disorders of muscles ("arthrogryposis multiplex congenita (Q74.3)")G71.2 Congenital myopathies ("arthrogryposis multiplex congenita (Q74.3)")G72 Other and unspecified myopathies ("arthrogryposis multiplex congenita (Q74.3)")M20 Acquired deformities of fingers and toes ("congenital deformities and malformations of fingers and toes (Q66.-, Q68-Q70, Q74.-)")M21 Other acquired deformities of limbs ("congenital deformities and malformations of limbs (Q65-Q66, Q68-Q74)")M24.3 Pathological dislocation of joint, not elsewhere classified ("congenital dislocation or displacement of joint- see congenital malformations and deformations of the musculoskeletal system (Q65-Q79)")M95 Other acquired deformities of musculoskeletal system and connective tissue ("congenital malformations and deformations of the musculoskeletal system (Q65-Q79)")Q74 Other congenital malformations of limb(s)Q74.0 Other congenital malformations of upper limb(s), including shoulder girdleQ74.1 Congenital malformation of kneeQ74.2 Other congenital malformations of lower limb(s), including pelvic girdleQ74.3 Arthrogryposis multiplex congenita (this code)Q74.8 Other specified congenital malformations of limb(s)Q74.9 Unspecified congenital malformation of limb(s)