ICD-10-CM Alphabetic Index · FY 2027 64 Entries
Short in the ICD-10-CM Index ICD-10-CM
The main term Short, shortening, shortness carries 64 index entries pointing to 26 ICD-10-CM codes. Every indented line below refines the term by site, cause, or type. Verify any candidate code in the Tabular List before using it.
✓ Built from the official CMS FY 2027 index fileEffective Oct 1, 2026 – Sep 30, 2027
64
Index Entries
26
Codes Referenced
—
Default Code
S
Letter
64 of 64 shown
ICD-10-CM
Index Entries Under Short 64 entries · 26 codes
Short, shortening, shortness
arm (acquired) see also Deformity, limb, unequal length
congenital Q71.81 Non-billable
forearm see Deformity, limb, unequal length
bowel syndrome see Syndrome, short bowel
breath R06.02
cervical (complicating pregnancy) O26.87 Non-billable
non-gravid uterus N88.3
common bile duct, congenital Q44.5
cord (umbilical), complicating delivery O69.3 Non-billable
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 Non-billable
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 Non-billable
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 Non-billable
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 Non-billable
upper limb, congenital see Defect, reduction, upper limb, specified type NEC
urethra N36.8
uvula, congenital Q38.5
vagina (congenital) Q52.4
The info icon previews the code's description and billable status; the code link opens its full page with all notations.
Related Index Terms
Source: Centers for Medicare & Medicaid Services, FY 2027 ICD-10-CM Index to Diseases and Injuries release files, effective October 1, 2026 through September 30, 2027.
