ICD-10-CM Alphabetic Index to Diseases and Injuries
Defect, defective
Default code: Q89.9. Follow the subterms below to reach a more specific code.ICD-10 code for Defect — guide and common questions →
- 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 Q21.10
- coronary sinus Q21.13
- following acute myocardial infarction (current complication) I23.1
- ostium primum type (type I) Q21.20
- with
- common atrioventricular valves and moderate or larger inlet VSD Q21.23
- separate atrioventricular valves Q21.21
- and small or restrictive inlet VSD Q21.22
- ostium secundum type (patent persistent) (type II) Q21.11
- sinus venosus Q21.16
- inferior Q21.15
- superior Q21.14
- specified NEC Q21.19
- vena cava type
- inferior Q21.15
- superior Q21.14
- atrioventricular
- canal Q21.20
- septal
- common Q21.23
- complete Q21.23
- incomplete Q21.21
- intermediate Q21.22
- partial Q21.21
- transitional Q21.22
- unspecified as to partial or complete Q21.20
- septum Q21.20
- auricular septal Q21.10
- bilirubin excretion NEC E80.6
- biosynthesis, androgen (testicular) E29.1
- bulbar septum Q21.0
- catalase E80.3
- cell membrane receptor complex (CR3) D71.8
- circulation I99.9
- congenital Q28.9
- newborn Q28.9
- coagulation (factor) D68.9 — see also Deficiency, factor
- with
- COVID-19 associated coagulopathy D68.8
- 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 O99.13
- with hemorrhage 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 Q21.13
- cushion, endocardial Q21.20
- common Q21.23
- incomplete Q21.21
- intermediate Q21.22
- transitional Q21.22
- 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 R93.41
- kidney R93.42-
- renal pelvis R93.41
- stomach R93.3
- ureter R93.41
- urinary organs, specified NEC R93.49
- GABA (gamma aminobutyric acid) metabolic E72.81
- Gerbode Q21.0
- glucose transport, blood-brain barrier E74.810
- glycoprotein degradation E77.1
- Hageman (factor) D68.2
- hearing — see Deafness
- high grade F70
- home, technical, preventing adequate care Z59.19
- interatrial septal Q21.19
- interauricular septal Q21.19
- interventricular septal Q21.0
- with dextroposition of aorta, pulmonary stenosis and hypertrophy of right ventricle Q21.3
- in tetralogy of Fallot Q21.3
- intervertebral annular fibrosis M51.9 — see also Disease, intervertebral disc, by site
- lumbar M51.A0
- large M51.A2
- small M51.A1
- lumbosacral M51.A3
- large M51.A5
- small M51.A4
- 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 Q21.20
- secundum Q21.11
- peroxidase E80.3
- placental blood supply — see Insufficiency, placental
- platelets, qualitative D69.19
- 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 D68.020 — see also Disease, von Willebrand
- defective platelet adhesion with a normal size distribution of von Willebrand factor multimers D68.022 — see also Disease, von Willebrand
- defective von Willebrand factor to factor VIII binding D68.023 — see also Disease, von Willebrand
- high-molecular-weight von Willebrand factor loss D68.021 — see also Disease, von Willebrand
- hyper-adhesive forms D68.021 — see also Disease, von Willebrand
- increased affinity for platelet glycoprotein lb D68.021 — see also Disease, von Willebrand
- markedly decreased affinity for factor VIII D68.023 — see also Disease, von Willebrand
- in von Willebrand factor function, with no further subtyping D68.029 — see also Disease, von Willebrand
- 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 Q21.10 — see also Defect, atrial septal
- 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 Q21.16 — see also Defect, atrial septal, sinus venosus
- speech — see Disorder, speech
- 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