ICD 10 CM Index: Defect, defective
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Defect, defective
ICD 10 Code is 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
- atrioventricular
- 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
- coagulation (factor) D68.9, See also Deficiency, factor
- with
- acquired D68.4
- antepartum with hemorrhage, See Hemorrhage, antepartum, with coagulation defect
- due to
- 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 Q21.1
- 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
- ectodermal, congenital Q82.9
- Eisenmenger's Q21.8
- enzyme
- 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 metabolic (gamma aminobutyric acid) 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
- 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
- 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
- specified type NEC Q72.89-
- split foot Q72.7-
- absence, See Agenesis, leg
- 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
- specified type NEC Q71.89-
- absence, See Agenesis, arm
- lower Q72.9-
- 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 NOS (heart) 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, See Disorder, speech
- 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
- generalized contraction H53.48-
- localized
- voice R49.9
- specified NEC R49.8
- wedge, tooth, teeth (abrasion) K03.1