Defect, defective
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 following acute myocardial infarction (current complication)
I23.1 ostium primum type
Q21.2 atrioventricular
canal
Q21.2 septum
Q21.2 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 congenital
Q28.9 newborn
Q28.9 coagulation (factor) --see also Deficiency, factor
D68.9 with
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
Q21.1 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 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 metabolic (gamma aminobutyric acid)
E72.81 Gerbode
Q21.0 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 --see also Deformity
M95.8 ostium
primum
Q21.2 secundum
Q21.1 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
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 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 --see also Defect, ventricular septal
Q21.0 sinus venosus
Q21.1 speech
R47.9 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