ICD-10-CM Short, shortening, shortness References

"Short, shortening, shortness" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries

Browse the ICD-10-CM codes with references applicable to the clinical term "short, shortening, shortness"

• Short, shortening, shortness
  • arm (acquired) - See Also: Deformity, limb, unequal length;
    • congenital - Q71.81 Congenital shortening of upper limb
    • forearm - See: Deformity, limb, unequal length;
  • bowel syndrome - K91.2 Postsurgical malabsorption, not elsewhere classified
  • breath - R06.02 Shortness of breath
  • cervical (complicating pregnancy) - O26.87 Cervical shortening
    • non-gravid uterus - N88.3 Incompetence of cervix uteri
  • common bile duct, congenital - Q44.5 Other congenital malformations of bile ducts
  • cord (umbilical), complicating delivery - O69.3 Labor and delivery complicated by short cord
  • cystic duct, congenital - Q44.5 Other congenital malformations of bile ducts
  • esophagus (congenital) - Q39.8 Other congenital malformations of esophagus
  • femur (acquired) - See: Deformity, limb, unequal length, femur;
    • congenital - See: Defect, reduction, lower limb, longitudinal, femur;
  • frenum, frenulum, linguae (congenital) - Q38.1 Ankyloglossia
  • hip (acquired) - See Also: Deformity, limb, unequal length;
    • congenital - Q65.89 Other specified congenital deformities of hip
  • leg (acquired) - See Also: Deformity, limb, unequal length;
    • congenital - Q72.81 Congenital shortening of lower limb
    • lower leg - See Also: Deformity, limb, unequal length;
  • limbed stature, with immunodeficiency - D82.2 Immunodeficiency with short-limbed stature
  • lower limb (acquired) - See Also: Deformity, limb, unequal length;
    • congenital - Q72.81 Congenital shortening of lower limb
  • organ or site, congenital NEC - See: Distortion;
  • palate, congenital - Q38.5 Congenital malformations of palate, not elsewhere classified
  • radius (acquired) - See Also: Deformity, limb, unequal length;
    • congenital - See: Defect, reduction, upper limb, longitudinal, radius;
  • rib syndrome - Q77.2 Short rib syndrome
  • stature (child) (hereditary) (idiopathic) NEC - R62.52 Short stature (child)
    • constitutional - E34.31 Constitutional short stature
    • due to
      • endocrine disorder - E34.30 Short stature due to endocrine disorder, unspecified
        • specified type NEC, due to endocrine disorder - E34.39 Other short stature due to endocrine disorder
      • genetic causes - E34.329 Unspecified genetic causes of short stature
        • ACAN gene variant - E34.328 Other genetic causes of short stature
        • acid-labile subunit gene (IGFALS) defect - E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
        • aggrecan deficiency - E34.328 Other genetic causes of short stature
        • genetic syndrome with resistance to insulin-like growth factor-1 - E34.322 Insulin-like growth factor-1 (IGF-1) resistance
        • growth hormone gene 1 (GH1) defect with growth hormone neutralizing antibodies - E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
        • growth hormone insensitivity syndrome (GHIS) - E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
        • insulin-like growth factor 1 gene (IGF1) defect - E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
        • insulin-like growth factor-1 (IGF-1) resistance - E34.322 Insulin-like growth factor-1 (IGF-1) resistance
        • insulin-like growth factor-1 receptor (IGF-1R) defect - E34.322 Insulin-like growth factor-1 (IGF-1) resistance
        • NPR-2 gene variant - E34.328 Other genetic causes of short stature
        • post-insulin-like growth factor-1 receptor signaling defect - E34.322 Insulin-like growth factor-1 (IGF-1) resistance
        • primary insulin-like growth factor-1 (IGF-1) deficiency - E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
        • severe primary insulin-like growth factor-1 deficiency (SPIGFD) - E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
        • signal transducer and activator of transcription 5B gene (STAT5b) defect - E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
        • specified genetic cause NEC - E34.328 Other genetic causes of short stature
    • Laron-type - E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
  • tendon - See Also: Contraction, tendon;
    • Achilles (acquired) - M67.0 Short Achilles tendon (acquired)
      • congenital - Q66.89 Other specified congenital deformities of feet
    • congenital - Q79.8 Other congenital malformations of musculoskeletal system
    • with contracture of joint - See: Contraction, joint;
  • 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 Labor and delivery complicated by short cord
  • upper limb, congenital - See: Defect, reduction, upper limb, specified type NEC;
  • urethra - N36.8 Other specified disorders of urethra
  • uvula, congenital - Q38.5 Congenital malformations of palate, not elsewhere classified
  • vagina (congenital) - Q52.4 Other congenital malformations of vagina