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2009 ICD-9-CM
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Hypoplasia, hypoplasis 759.89 | |
cartilaginous 756.9 | |
cecum 751.2 | |
cementum 520.4 | |
hereditary 520.5 | |
cephalic 742.1 | |
cerebellum 742.2 | |
cervix (uteri) 752.49 | |
chin 524.06 | |
clavicle 755.51 | |
coccyx 756.19 | |
colon 751.2 | |
corpus callosum 742.2 | |
cricoid cartilage 748.3 | |
dermal, focal (Goltz) 757.39 | |
digestive organ(s) or tract NEC 751.8 | |
lower 751.2 | |
upper 750.8 | |
ear 744.29 | |
auricle 744.23 | |
lobe 744.29 | |
middle, except ossicles 744.03 | |
ossicles 744.04 | |
ossicles 744.04 | |
enamel of teeth (neonatal) (postnatal) (prenatal) 520.4 | |
hereditary 520.5 | |
endocrine (gland) NEC 759.2 | |
endometrium 621.8 | |
epididymis 752.89 | |
epiglottis 748.3 | |
erythroid, congenital 284.01 | |
erythropoietic, chronic acquired 284.81 | |
esophagus 750.3 | |
Eustachian tube 744.24 | |
eye (see also Microphthalmos) 743.10 | |
lid 743.62 | |
face 744.89 | |
bone(s) 756.0 | |
fallopian tube 752.19 | |
femur (see also Absence, femur, congenital) 755.34 | |
fibula (see also Absence, fibula, congenital) 755.37 | |
finger (see also Absence, finger, congenital) 755.29 | |
focal dermal 757.39 | |
foot 755.31 | |
gallbladder 751.69 | |
genitalia, genital organ(s) | |
female 752.89 | |
external 752.49 | |
internal NEC 752.89 | |
in adiposogenital dystrophy 253.8 | |
male 752.89 | |