ICD-10 code lookup
ICD-10-CM
Defect, defective
The ICD-10-CM index points "Defect, defective" to Q89.9, Congenital malformation, unspecified.
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Index
- E25.03-beta-hydroxysteroid dehydrogenase, Congenital adrenogenital disorders associated with enzyme deficiency
- E25.011-hydroxylase, Congenital adrenogenital disorders associated with enzyme deficiency
- E25.021-hydroxylase, Congenital adrenogenital disorders associated with enzyme deficiency
- Q79.59abdominal wall, congenital, Other congenital malformations of abdominal wall
- D80.9antibody immunodeficiency, Immunodeficiency with predominantly antibody defects, unspecified
- Q21.4aorticopulmonary septum, Aortopulmonary septal defect
- Q21.10atrial septal, Atrial septal defect, unspecified
- Q21.10auricular septal, Atrial septal defect, unspecified
- E80.6bilirubin excretion NEC, Other disorders of bilirubin metabolism
- E29.1biosynthesis, androgen(testicular), Testicular hypofunction
- Q21.0bulbar septum, Ventricular septal defect
- E80.3catalase, Defects of catalase and peroxidase
- D71.8cell membrane receptor complex(CR3), Other functional disorders of polymorphonuclear neutrophils
- I99.9circulation, Unspecified disorder of circulatory system
- D68.9coagulation(factor), Coagulation defect, unspecified
- D84.1complement system, Defects in the complement system
- I45.9conduction(heart), Conduction disorder, unspecified
- Q21.13coronary sinus, Coronary sinus atrial septal defect
- Q21.20cushion, endocardial, Atrioventricular septal defect, unspecified as to partial or complete
- E77.1degradation, glycoprotein, Defects in glycoprotein degradation
- K08.50dental restoration, Unsatisfactory restoration of tooth, unspecified
- K00.5dentin(hereditary), Hereditary disturbances in tooth structure, not elsewhere classified
- Q13.89Descemet's membrane, congenital, Other congenital malformations of anterior segment of eye
- Q82.9ectodermal, congenital, Congenital malformation of skin, unspecified
- Q21.8Eisenmenger's, Other congenital malformations of cardiac septa
- Q39.9esophagus, congenital, Congenital malformation of esophagus, unspecified
- M62.89extensor retinaculum, Other specified disorders of muscle
- D68.2fibrin polymerization, Hereditary deficiency of other clotting factors
- E72.81GABA(gamma aminobutyric acid) metabolic, Disorders of gamma aminobutyric acid metabolism
- Q21.0Gerbode, Ventricular septal defect
- E74.810glucose transport, blood-brain barrier, Glucose transporter protein type 1 deficiency
- E77.1glycoprotein degradation, Defects in glycoprotein degradation
- D68.2Hageman(factor), Hereditary deficiency of other clotting factors
- F70high grade, Mild intellectual disabilities
- Z59.19home, technical, preventing adequate care, Other inadequate housing
- Q21.19interatrial septal, Other specified atrial septal defect
- Q21.19interauricular septal, Other specified atrial septal defect
- Q21.0interventricular septal, Ventricular septal defect
- M51.9intervertebral annular fibrosis, Unspecified thoracic, thoracolumbar and lumbosacral intervertebral disc disorder
- D84.0lymphocyte function antigen-1(LFA-1), Lymphocyte function antigen-1 [LFA-1] defect