Short, shortening, shortness - in the ICD-10-CM Index

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

Tendons: Fibrous bands or cords of CONNECTIVE TISSUE at the ends of SKELETAL MUSCLE FIBERS that serve to attach the MUSCLES to bones and other structures.

Umbilical Cord: The flexible rope-like structure that connects a developing FETUS to the PLACENTA in mammals. The cord contains blood vessels which carry oxygen and nutrients from the mother to the fetus and waste products away from the fetus.

Urethra: A tube that transports URINE from the URINARY BLADDER to the outside of the body in both the sexes. It also has a reproductive function in the male by providing a passage for SPERM.