Instruction manual part 2e, vol 3: ICD-10 index

INTERNATIONAL CLASSIFICATION OF DISEASES
Defect—continued
- lymphocyte function antigen-1 (LFA-1)
D84.0
- lysosomal enzyme, post-translational
modification E77.0
- mental - see Retardation, mental
- metabolic E88.9
- - congenital E88.9
- modification, lysosomal enzymes,
post-translational E77.0
- neural tube Q07.9
- ostium
- - primum Q21.2
- - secundum Q21.1
- peroxidase E80.3
- placental blood supply - see Insufficiency,
placental
- platelets, qualitative D69.1
- postural NEC, spine M43.9
- renal pelvis Q63.8
- - obstructive Q62.3
- respiratory system, congenital Q34.9
- septal (heart) NEC Q21.9
- - acquired (atrial) (auricular) (ventricular)
(old) I51.0
- - atrial (see also Defect, atrial, septal) Q21.1
- - ventricular (see also Defect, ventricular
septal) Q21.0
- sinus venosus Q21.1
- speech NEC R47.8
- - developmental F80.9
- vascular (local) I99
- - congenital Q27.9
- ventricular septal Q21.0
- - in tetralogy of Fallot Q21.3
- vision NEC H54.7
- visual field H53.4
- voice R49.8
- wedge, tooth, teeth (abrasion) K03.1
Deferentitis N49.1
- gonorrheal (acute) (chronic) A54.2† N51.8*
Defibrination (syndrome) D65
- antepartum O46.0
- - affecting fetus or newborn P02.1
- fetus or newborn P60
- following
- - abortion (subsequent episode) O08.1
- - - current episode - see Abortion
- - ectopic or molar pregnancy O08.1
- intrapartum O67.0
- postpartum O72.3
- pregnancy NEC O46.0
Deficiency, deficient
- abdominal muscle syndrome Q79.4
- AC globulin (congenital) (hereditary) D68.2
- - acquired D68.4
- acetyl CoA dehydrogenase E71.3
- acid phosphatase E83.3
- acyl CoA dehydrogenase E71.3
- adenosine deaminase (ADA) D81.3
- aldolase (hereditary) E74.1
- amino-acids E72.9
- anemia - see Anemia
- aneurin E51.9
- antibody with
- - hyperimmunoglobulinemia D80.6
- - near-normal immunoglobins D80.6
- antidiuretic hormone secretion
(inappropriate) E22.2
- anti-hemophilic globulin NEC D66
- antithrombin III D68.8
- α-1-antitrypsin E88.0
- ascorbic acid E54
- attention (disorder) (syndrome) F98.8
- - with hyperactivity F90.0
- autoimmune M35.9
- bile salt K90.8
- biotin E53.8
- biotin-dependent carboxylase D81.8
- brancher enzyme (amylopectinosis) E74.0
D-6