Index to Diseases and Injuries
Short, shortening, shortness
- arm (acquired) — see also Deformity, limb, unequal length
- congenital Q71.81-
- forearm — see Deformity, limb, unequal length
- bowel syndrome — see Syndrome, short bowel
- breath R06.02
- cervical (complicating pregnancy) O26.87-
- non-gravid uterus N88.3
- common bile duct, congenital Q44.5
- cord (umbilical) , complicating delivery O69.3
- cystic duct, congenital Q44.5
- esophagus (congenital) Q39.8
- femur (acquired) — see Deformity, limb, unequal length, femur
- congenital — see Defect, reduction, lower limb, longitudinal, femur
- frenum, frenulum, linguae (congenital) Q38.1
- hip (acquired) — see also Deformity, limb, unequal length
- congenital Q65.89
- leg (acquired) — see also Deformity, limb, unequal length
- congenital Q72.81-
- lower leg — see also Deformity, limb, unequal length
- limbed stature, with immunodeficiency D82.2
- lower limb (acquired) — see also Deformity, limb, unequal length
- congenital Q72.81-
- organ or site, congenital NEC — see Distortion
- palate, congenital Q38.5
- radius (acquired) — see also Deformity, limb, unequal length
- congenital — see Defect, reduction, upper limb, longitudinal, radius
- rib syndrome Q77.2
- stature (child) (hereditary) (idiopathic) NEC R62.52
- constitutional E34.31
- due to
- endocrine disorder E34.30
- specified type NEC, due to endocrine disorder E34.39
- genetic causes E34.329
- ACAN gene variant E34.328
- acid-labile subunit gene (IGFALS) defect E34.321
- aggrecan deficiency E34.328
- genetic syndrome with resistance to insulin-like growth factor-1 E34.322
- growth hormone gene 1 (GH1) defect with growth hormone neutralizing antibodies E34.321
- growth hormone insensitivity syndrome (GHIS) E34.321
- insulin-like growth factor 1 gene (IGF1) defect E34.321
- insulin-like growth factor-1 receptor (IGF-1R) defect E34.322
- insulin-like growth factor-1 (IGF-1) resistance E34.322
- NPR-2 gene variant E34.328
- post-insulin-like growth factor-1 receptor signaling defect E34.322
- primary insulin-like growth factor-1 (IGF-1) deficiency E34.321
- severe primary insulin-like growth factor-1 deficiency (SPIGFD) E34.321
- signal transducer and activator of transcription 5B gene (STAT5b) defect E34.321
- specified genetic cause NEC E34.328
- Laron-type E34.321
- tendon — see also Contraction, tendon
- with contracture of joint — see Contraction, joint
- Achilles (acquired) M67.0-
- congenital Q66.89
- congenital Q79.8
- thigh (acquired) — see also Deformity, limb, unequal length, femur
- congenital — see Defect, reduction, lower limb, longitudinal, femur
- tibialis anterior (tendon) — see Contraction, tendon
- umbilical cord
- complicating delivery O69.3
- upper limb, congenital — see Defect, reduction, upper limb, specified type NEC
- urethra N36.8
- uvula, congenital Q38.5
- vagina (congenital) Q52.4
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.