Alphabetic Index · main term

Defect, defective

FY2027Index: De /Alphabetic Index

At the main termQ89.9

Defect, defective is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists Q89.9 for the term on its own. It has 259 subterms and 221 code entries. First-level subterms include 3-beta-hydroxysteroid dehydrogenase, 11-hydroxylase, 21-hydroxylase, abdominal wall, congenital, antibody immunodeficiency, aorticopulmonary septum, atrial septal, atrioventricular and more. Confirm any code you find here in the Tabular List before you report it.

Subterms 259

3-beta-hydroxysteroid dehydrogenaseE25.0
11-hydroxylaseE25.0
21-hydroxylaseE25.0
abdominal wall, congenitalQ79.59
antibody immunodeficiencyD80.9
aorticopulmonary septumQ21.4
atrial septalQ21.10
- coronary sinusQ21.13
- following acute myocardial infarction (current complication)I23.1
- ostium primum type (type I)Q21.20
  - with
    common atrioventricular valves and moderate or larger inlet VSDQ21.23
    separate atrioventricular valvesQ21.21
    and small or restrictive inlet VSDQ21.22
- ostium secundum type (patent persistent) (type II)Q21.11
- sinus venosusQ21.16
  - inferiorQ21.15
  - superiorQ21.14
- specified NECQ21.19
- vena cava type
  - inferiorQ21.15
  - superiorQ21.14
atrioventricular
- canalQ21.20
- septal
  - commonQ21.23
  - completeQ21.23
  - incompleteQ21.21
  - intermediateQ21.22
  - partialQ21.21
  - transitionalQ21.22
  - unspecified as to partial or completeQ21.20
- septumQ21.20
auricular septalQ21.10
bilirubin excretion NECE80.6
biosynthesis, androgen (testicular)E29.1
bulbar septumQ21.0
catalaseE80.3
cell membrane receptor complex (CR3)D71.8
circulationI99.9
- congenitalQ28.9
- newbornQ28.9
coagulation (factor) see also Deficiency, factorD68.9
- with
  - COVID-19 associated coagulopathyD68.8
  - ectopic pregnancyO08.1
  - molar pregnancyO08.1
- acquiredD68.4
- antepartum with hemorrhage see Hemorrhage, antepartum, with coagulation defect
- due to
  - liver diseaseD68.4
  - vitamin K deficiencyD68.4
- hereditary NECD68.2
- intrapartumO67.0
- newborn, transientP61.6
- postpartumO99.13
  - with hemorrhageO72.3
- specified type NECD68.8
complement systemD84.1
conduction (heart)I45.9
- bone see Deafness, conductive
congenital, organ or site not listed see Anomaly, by site
coronary sinusQ21.13
cushion, endocardialQ21.20
- commonQ21.23
- incompleteQ21.21
- intermediateQ21.22
- transitionalQ21.22
degradation, glycoproteinE77.1
dental bridge, crown, fillings see Defect, dental restoration
dental restorationK08.50
- specified NECK08.59
dentin (hereditary)K00.5
Descemet's membrane, congenitalQ13.89
developmental see also Anomaly
- cauda equinaQ06.3
diaphragm
- with elevation, eventration or hernia see Hernia, diaphragm
- congenitalQ79.1
  - with herniaQ79.0
  - gross (with hernia)Q79.0
ectodermal, congenitalQ82.9
Eisenmenger'sQ21.8
enzyme
- catalaseE80.3
- peroxidaseE80.3
esophagus, congenitalQ39.9
extensor retinaculumM62.89
fibrin polymerizationD68.2
filling
- bladderR93.41
- kidneyR93.42-
- renal pelvisR93.41
- stomachR93.3
- ureterR93.41
- urinary organs, specified NECR93.49
GABA (gamma aminobutyric acid) metabolicE72.81
GerbodeQ21.0
glucose transport, blood-brain barrierE74.810
glycoprotein degradationE77.1
Hageman (factor)D68.2
hearing see Deafness
high gradeF70
home, technical, preventing adequate careZ59.19
interatrial septalQ21.19
interauricular septalQ21.19
interventricular septalQ21.0
- with dextroposition of aorta, pulmonary stenosis and hypertrophy of right ventricleQ21.3
- in tetralogy of FallotQ21.3
intervertebral annular fibrosis see also Disease, intervertebral disc, by siteM51.9
- lumbarM51.A0
  - largeM51.A2
  - smallM51.A1
- lumbosacralM51.A3
  - largeM51.A5
  - smallM51.A4
learning (specific) see Disorder, learning
lymphocyte function antigen-1 (LFA-1)D84.0
lysosomal enzyme, post-translational modificationE77.0
major osseousM89.70
- ankleM89.77-
- carpusM89.74-
- clavicleM89.71-
- femurM89.75-
- fibulaM89.76-
- fingersM89.74-
- footM89.77-
- forearmM89.73-
- handM89.74-
- humerusM89.72-
- lower legM89.76-
- metacarpusM89.74-
- metatarsusM89.77-
- multiple sitesM89.79
- pelvic regionM89.75-
- pelvisM89.75-
- radiusM89.73-
- scapulaM89.71-
- shoulder regionM89.71-
- specified NECM89.78
- tarsusM89.77-
- thighM89.75-
- tibiaM89.76-
- toesM89.77-
- ulnaM89.73-
mental see Disability, intellectual
modification, lysosomal enzymes, post-translationalE77.0
obstructive, congenital
- renal pelvisQ62.39
- ureterQ62.39
  - atresia see Atresia, ureter
  - cecoureteroceleQ62.32
  - megaureterQ62.2
  - orthotopic ureteroceleQ62.31
osseous, majorM89.70
- ankleM89.77-
- carpusM89.74-
- clavicleM89.71-
- femurM89.75-
- fibulaM89.76-
- fingersM89.74-
- footM89.77-
- forearmM89.73-
- handM89.74-
- humerusM89.72-
- lower legM89.76-
- metacarpusM89.74-
- metatarsusM89.77-
- multiple sitesM89.9
- pelvic regionM89.75-
- pelvisM89.75-
- radiusM89.73-
- scapulaM89.71-
- shoulder regionM89.71-
- specified NECM89.78
- tarsusM89.77-
- thighM89.75-
- tibiaM89.76-
- toesM89.77-
- ulnaM89.73-
osteochondral NEC see also DeformityM95.8
ostium
- primumQ21.20
- secundumQ21.11
peroxidaseE80.3
placental blood supply see Insufficiency, placental
platelets, qualitativeD69.19
- constitutional see Disease, von Willebrand
postural NEC, spine see Dorsopathy, deforming
qualitative, of von Willebrand factor
- with
  - decreased platelet adhesion and selective deficiency of high-molecular-weight multimers see also Disease, von WillebrandD68.020
  - defective platelet adhesion with a normal size distribution of von Willebrand factor multimers see also Disease, von WillebrandD68.022
  - defective von Willebrand factor to factor VIII binding see also Disease, von WillebrandD68.023
  - high-molecular-weight von Willebrand factor loss see also Disease, von WillebrandD68.021
  - hyper-adhesive forms see also Disease, von WillebrandD68.021
  - increased affinity for platelet glycoprotein lb see also Disease, von WillebrandD68.021
  - markedly decreased affinity for factor VIII see also Disease, von WillebrandD68.023
- in von Willebrand factor function, with no further subtyping see also Disease, von WillebrandD68.029
reduction
- limbQ73.8
  - lowerQ72.9-
    absence see Agenesis, leg
    foot see Agenesis, foot
    longitudinal
    femurQ72.4-
    fibulaQ72.6-
    tibiaQ72.5-
    specified type NECQ72.89-
    split footQ72.7-
  - specified type NECQ73.8
  - upperQ71.9-
    absence see Agenesis, arm
    forearm see Agenesis, forearm
    hand see Agenesis, hand
    lobster-claw handQ71.6-
    longitudinal
    radiusQ71.4-
    ulnaQ71.5-
    specified type NECQ71.89-
renal pelvisQ63.8
- obstructiveQ62.39
respiratory system, congenitalQ34.9
restoration, dentalK08.50
- specified NECK08.59
retinal nerve bundle fibersH35.89
septal (heart) NOSQ21.9
- acquired (atrial) (auricular) (ventricular) (old)I51.0
- atrial see also Defect, atrial septalQ21.10
  - concurrent with acute myocardial infarction see Infarct, myocardium
  - following acute myocardial infarction (current complication)I23.1
- ventricular see also Defect, ventricular septalQ21.0
sinus venosus see also Defect, atrial septal, sinus venosusQ21.16
speech see Disorder, speech
- developmentalF80.9
- specified NECR47.89
Taussig-Bing (aortic transposition and overriding pulmonary artery)Q20.1
teeth, wedgeK03.1
vascular (local)I99.9
- congenitalQ27.9
ventricular septalQ21.0
- concurrent with acute myocardial infarction see Infarct, myocardium
- following acute myocardial infarction (current complication)I23.2
- in tetralogy of FallotQ21.3
vision NECH54.7
visual fieldH53.40
- bilateral
  - heteronymousH53.47
  - homonymousH53.46-
- generalized contractionH53.48-
- localized
  - arcuateH53.43-
  - scotoma (central area)H53.41-
    blind spot areaH53.42-
  - sectorH53.43-
  - specified type NECH53.45-
voiceR49.9
- specified NECR49.8
wedge, tooth, teeth (abrasion)K03.1