Alphabetic index · S

Short, shortening, shortness

Sub-terms

arm (acquired)see also Deformity, limb, unequal length
congenitalQ71.81-needs more characters
forearmsee Deformity, limb, unequal length
bowel syndromesee Syndrome, short bowel
breathR06.02
cervical (complicating pregnancy)O26.87-needs more characters
non-gravid uterusN88.3
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
congenitalsee 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-needs more characters
lower legsee also Deformity, limb, unequal length
limbed stature, with immunodeficiencyD82.2
lower limb (acquired)see also Deformity, limb, unequal length
congenitalQ72.81-needs more characters
organ or site, congenital NECsee Distortion
palate, congenitalQ38.5
radius (acquired)see also Deformity, limb, unequal length
congenitalsee Defect, reduction, upper limb, longitudinal, radius
rib syndromeQ77.2
stature (child) (hereditary) (idiopathic) NECR62.52
constitutionalE34.31
due to
endocrine disorderE34.30
specified type NEC, due to endocrine disorderE34.39
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
tendonsee also Contraction, tendon
with contracture of jointsee Contraction, joint
Achilles (acquired)M67.0-needs more characters
congenitalQ66.89
congenitalQ79.8
thigh (acquired)see also Deformity, limb, unequal length, femur
congenitalsee Defect, reduction, lower limb, longitudinal, femur
tibialis anterior (tendon)see Contraction, tendon
umbilical cord
complicating deliveryO69.3
upper limb, congenitalsee Defect, reduction, upper limb, specified type NEC
urethraN36.8
uvula, congenitalQ38.5
vagina (congenital)Q52.4

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