Defect ICD-10-CM Alphabetical Index

The ICD-10-CM Alphabetical Index is designed to allow medical coders to look up various medical terms and connect them with the appropriate ICD codes. There are 73 terms under the parent term 'Defect' in the ICD-10-CM Alphabetical Index.

Defect

See Code: Q89.9

3-beta-hydroxysteroid dehydrogenase E25.0

11-hydroxylase E25.0

21-hydroxylase E25.0

abdominal wall, congenital Q79.59

antibody immunodeficiency D80.9

aorticopulmonary septum Q21.4

atrial septal (ostium secundum type) Q21.1
following acute myocardial infarction (current complication) I23.1
ostium primum type Q21.2
atrioventricular
canal Q21.2
septum Q21.2
auricular septal Q21.1
bilirubin excretion NEC E80.6
biosynthesis, androgen (testicular) E29.1
bulbar septum Q21.0
catalase E80.3
cell membrane receptor complex (CR3) D71
circulation I99.9
congenital Q28.9
newborn Q28.9
coagulation (factor) D68.9 - see also Deficiency, factor
with
ectopic pregnancy O08.1
molar pregnancy O08.1
acquired D68.4
antepartum with hemorrhage - see Hemorrhage, antepartum, with coagulation defect
due to
liver disease D68.4
vitamin K deficiency D68.4
hereditary NEC D68.2
intrapartum O67.0
newborn, transient P61.6
postpartum O72.3
specified type NEC D68.8
complement system D84.1
conduction (heart) I45.9
bone - see Deafness, conductive
congenital, organ or site not listed - see Anomaly, by site
coronary sinus Q21.1
cushion, endocardial Q21.2
degradation, glycoprotein E77.1
dental bridge, crown, fillings - see Defect, dental restoration
dental restoration K08.50
specified NEC K08.59
dentin (hereditary) K00.5
Descemet's membrane, congenital Q13.89
developmental - see also Anomaly
cauda equina Q06.3
diaphragm
with elevation, eventration or hernia - see Hernia, diaphragm
congenital Q79.1
with hernia Q79.0
gross (with hernia) Q79.0
ectodermal, congenital Q82.9
Eisenmenger's Q21.8
enzyme
catalase E80.3
peroxidase E80.3
esophagus, congenital Q39.9
extensor retinaculum M62.89
fibrin polymerization D68.2
filling
bladder R93.4
kidney R93.4
stomach R93.3
ureter R93.4
Gerbode Q21.0
glycoprotein degradation E77.1
Hageman (factor) D68.2
hearing - see Deafness
high grade F70
interatrial septal Q21.1
interauricular septal Q21.1
interventricular septal Q21.0
with dextroposition of aorta, pulmonary stenosis and hypertrophy of right ventricle Q21.3
in tetralogy of Fallot Q21.3
learning (specific) - see Disorder, learning
lymphocyte function antigen-1 (LFA-1) D84.0
lysosomal enzyme, post-translational modification E77.0
major osseous M89.70
ankle M89.77-
carpus M89.74-
clavicle M89.71-
femur M89.75-
fibula M89.76-
fingers M89.74-
foot M89.77-
forearm M89.73-
hand M89.74-
humerus M89.72-
lower leg M89.76-
metacarpus M89.74-
metatarsus M89.77-
multiple sites M89.79
pelvic region M89.75-
pelvis M89.75-
radius M89.73-
scapula M89.71-
shoulder region M89.71-
specified NEC M89.78
tarsus M89.77-
thigh M89.75-
tibia M89.76-
toes M89.77-
ulna M89.73-
mental - see Disability, intellectual
modification, lysosomal enzymes, post-translational E77.0
obstructive, congenital
renal pelvis Q62.39
ureter Q62.39
atresia - see Atresia, ureter
cecoureterocele Q62.32
megaureter Q62.2
orthotopic ureterocele Q62.31
osseous, major M89.70
ankle M89.77-
carpus M89.74-
clavicle M89.71-
femur M89.75-
fibula M89.76-
fingers M89.74-
foot M89.77-
forearm M89.73-
hand M89.74-
humerus M89.72-
lower leg M89.76-
metacarpus M89.74-
metatarsus M89.77-
multiple sites M89.9
pelvic region M89.75-
pelvis M89.75-
radius M89.73-
scapula M89.71-
shoulder region M89.71-
specified NEC M89.78
tarsus M89.77-
thigh M89.75-
tibia M89.76-
toes M89.77-
ulna M89.73-
osteochondral NEC M95.8 - see also Deformity
ostium
primum Q21.2
secundum Q21.1
peroxidase E80.3
placental blood supply - see Insufficiency, placental
platelets, qualitative D69.1
constitutional D68.0
postural NEC, spine - see Dorsopathy, deforming
reduction
limb Q73.8
lower Q72.9-
absence - see Agenesis, leg
foot - see Agenesis, foot
longitudinal
femur Q72.4-
fibula Q72.6-
tibia Q72.5-
specified type NEC Q72.89-
split foot Q72.7-
specified type NEC Q73.8
upper Q71.9-
absence - see Agenesis, arm
forearm - see Agenesis, forearm
hand - see Agenesis, hand
lobster-claw hand Q71.6-
longitudinal
radius Q71.4-
ulna Q71.5-
specified type NEC Q71.89-
renal pelvis Q63.8
obstructive Q62.39
respiratory system, congenital Q34.9
restoration, dental K08.50
specified NEC K08.59
retinal nerve bundle fibers H35.89
septal (heart) NOS Q21.9
acquired (atrial) (auricular) (ventricular) (old) I51.0
atrial Q21.1
concurrent with acute myocardial infarction - see Infarct, myocardium
following acute myocardial infarction (current complication) I23.1
ventricular Q21.0 - see also Defect, ventricular septal
sinus venosus Q21.1
speech R47.9
developmental F80.9
specified NEC R47.89
Taussig-Bing (aortic transposition and overriding pulmonary artery) Q20.1
teeth, wedge K03.1
vascular (local) I99.9
congenital Q27.9
ventricular septal Q21.0
concurrent with acute myocardial infarction - see Infarct, myocardium
following acute myocardial infarction (current complication) I23.2
in tetralogy of Fallot Q21.3
vision NEC H54.7
visual field H53.40
bilateral
heteronymous H53.47
homonymous H53.46-
generalized contraction H53.48-
localized
arcuate H53.43-
scotoma (central area) H53.41-
blind spot area H53.42-
sector H53.43-
specified type NEC H53.45-
voice R49.9
specified NEC R49.8
wedge, tooth, teeth (abrasion) K03.1