Alphabetic Index · main term
Short, shortening, shortness
Short, shortening, shortness is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). It has 63 subterms and 43 code entries. First-level subterms include arm, bowel syndrome, breath, cervical, common bile duct, congenital, cord , complicating delivery, cystic duct, congenital, esophagus and more. Confirm any code you find here in the Tabular List before you report it.
Subterms 63
arm (acquired) see also Deformity, limb, unequal length
- congenitalQ71.81-
- forearm see Deformity, limb, unequal length
- bowel syndrome see Syndrome, short bowel
- breathR06.02
- common bile duct, congenitalQ44.5
- cord (umbilical), complicating deliveryO69.3
- cystic duct, congenitalQ44.5
- 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
- congenitalQ65.89
leg (acquired) see also Deformity, limb, unequal length
- congenitalQ72.81-
- lower leg see also Deformity, limb, unequal length
- limbed stature, with immunodeficiencyD82.2
lower limb (acquired) see also Deformity, limb, unequal length
- congenitalQ72.81-
- organ or site, congenital NEC see Distortion
- palate, congenitalQ38.5
radius (acquired) see also Deformity, limb, unequal length
- congenital see Defect, reduction, upper limb, longitudinal, radius
- rib syndromeQ77.2
stature (child) (hereditary) (idiopathic) NECR62.52
- constitutionalE34.31
due to
genetic causesE34.329
- ACAN gene variantE34.328
- acid-labile subunit gene (IGFALS) defectE34.321
- aggrecan deficiencyE34.328
- genetic syndrome with resistance to insulin-like growth factor-1E34.322
- growth hormone gene 1 (GH1) defect with growth hormone neutralizing antibodiesE34.321
- growth hormone insensitivity syndrome (GHIS)E34.321
- insulin-like growth factor 1 gene (IGF1) defectE34.321
- insulin-like growth factor-1 receptor (IGF-1R) defectE34.322
- insulin-like growth factor-1 (IGF-1) resistanceE34.322
- NPR-2 gene variantE34.328
- post-insulin-like growth factor-1 receptor signaling defectE34.322
- primary insulin-like growth factor-1 (IGF-1) deficiencyE34.321
- severe primary insulin-like growth factor-1 deficiency (SPIGFD)E34.321
- signal transducer and activator of transcription 5B gene (STAT5b) defectE34.321
- specified genetic cause NECE34.328
- Laron-typeE34.321
tendon see also Contraction, tendon
- with contracture of joint see Contraction, joint
- congenitalQ79.8
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 deliveryO69.3
- upper limb, congenital see Defect, reduction, upper limb, specified type NEC
- urethraN36.8
- uvula, congenitalQ38.5
- vagina (congenital)Q52.4