3-beta-hydroxysteroid dehydrogenaseE25.0

11-hydroxylaseE25.0

21-hydroxylaseE25.0

abdominal wall, congenitalQ79.59

antibody immunodeficiencyD80.9

aorticopulmonary septumQ21.4

atrial septalQ21.10

coronary sinusQ21.13

following acute myocardial infarction I23.1

ostium primum type Q21.20

with

common atrioventricular valves and moderate or larger inlet VSDQ21.23

separate atrioventricular valvesQ21.21

and small or restrictive inlet VSDQ21.22

ostium secundum type Q21.11

sinus venosusQ21.16

inferiorQ21.15

superiorQ21.14

specified NECQ21.19

vena cava type

inferiorQ21.15

superiorQ21.14

atrioventricular

canalQ21.20

septal

commonQ21.23

completeQ21.23

incompleteQ21.21

intermediateQ21.22

partialQ21.21

transitionalQ21.22

unspecified as to partial or completeQ21.20

septumQ21.20

auricular septalQ21.10

bilirubin excretion NECE80.6

biosynthesis, androgen E29.1

bulbar septumQ21.0

catalaseE80.3

cell membrane receptor complex D71

circulationI99.9

congenitalQ28.9

newbornQ28.9

coagulation , see also [Deficiency, factor]D68.9

with

COVID-19 associated coagulopathyD68.8

ectopic pregnancyO08.1

molar pregnancyO08.1

acquiredD68.4

antepartum with hemorrhage, see [Hemorrhage, antepartum, with coagulation defect]

due to

liver diseaseD68.4

vitamin K deficiencyD68.4

hereditary NECD68.2

intrapartumO67.0

newborn, transientP61.6

postpartumO99.13

with hemorrhageO72.3

specified type NECD68.8

complement systemD84.1

conduction I45.9

bone, see [Deafness, conductive]

congenital, organ or site not listed, see [Anomaly, by site]

coronary sinusQ21.13

cushion, endocardialQ21.20

commonQ21.23

incompleteQ21.21

intermediateQ21.22

transitionalQ21.22

degradation, glycoproteinE77.1

dental bridge, crown, fillings, see [Defect, dental restoration]

dental restorationK08.50

specified NECK08.59

dentin K00.5

Descemet's membrane, congenitalQ13.89

developmental, see also [Anomaly]

cauda equinaQ06.3

diaphragm

with elevation, eventration or hernia, see [Hernia, diaphragm]

congenitalQ79.1

with herniaQ79.0

gross Q79.0

ectodermal, congenitalQ82.9

Eisenmenger'sQ21.8

enzyme

catalaseE80.3

peroxidaseE80.3

esophagus, congenitalQ39.9

extensor retinaculumM62.89

fibrin polymerizationD68.2

filling

bladderR93.41

kidneyR93.42-

renal pelvisR93.41

stomachR93.3

ureterR93.41

urinary organs, specified NECR93.49

GABA metabolicE72.81

GerbodeQ21.0

glucose transport, blood-brain barrierE74.810

glycoprotein degradationE77.1

Hageman D68.2

hearing, see [Deafness]

high gradeF70

home, technical, preventing adequate careZ59.19

interatrial septalQ21.19

interauricular septalQ21.19

interventricular septalQ21.0

with dextroposition of aorta, pulmonary stenosis and hypertrophy of right ventricleQ21.3

in tetralogy of FallotQ21.3

intervertebral annular fibrosis, see also [Disease, intervertebral disc, by site]M51.9

lumbarM51.A0

largeM51.A2

smallM51.A1

lumbosacralM51.A3

largeM51.A5

smallM51.A4

learning , see [Disorder, learning]

lymphocyte function antigen-1 D84.0

lysosomal enzyme, post-translational modificationE77.0

major osseousM89.70

ankleM89.77-

carpusM89.74-

clavicleM89.71-

femurM89.75-

fibulaM89.76-

fingersM89.74-

footM89.77-

forearmM89.73-

handM89.74-

humerusM89.72-

lower legM89.76-

metacarpusM89.74-

metatarsusM89.77-

multiple sitesM89.79

pelvic regionM89.75-

pelvisM89.75-

radiusM89.73-

scapulaM89.71-

shoulder regionM89.71-

specified NECM89.78

tarsusM89.77-

thighM89.75-

tibiaM89.76-

toesM89.77-

ulnaM89.73-

mental, see [Disability, intellectual]

modification, lysosomal enzymes, post-translationalE77.0

obstructive, congenital

renal pelvisQ62.39

ureterQ62.39

atresia, see [Atresia, ureter]

cecoureteroceleQ62.32

megaureterQ62.2

orthotopic ureteroceleQ62.31

osseous, majorM89.70

ankleM89.77-

carpusM89.74-

clavicleM89.71-

femurM89.75-

fibulaM89.76-

fingersM89.74-

footM89.77-

forearmM89.73-

handM89.74-

humerusM89.72-

lower legM89.76-

metacarpusM89.74-

metatarsusM89.77-

multiple sitesM89.9

pelvic regionM89.75-

pelvisM89.75-

radiusM89.73-

scapulaM89.71-

shoulder regionM89.71-

specified NECM89.78

tarsusM89.77-

thighM89.75-

tibiaM89.76-

toesM89.77-

ulnaM89.73-

osteochondral NEC, see also [Deformity]M95.8

ostium

primumQ21.20

secundumQ21.11

peroxidaseE80.3

placental blood supply, see [Insufficiency, placental]

platelets, qualitativeD69.1

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, see also [Disease, von Willebrand]D68.020

defective platelet adhesion with a normal size distribution of von Willebrand factor multimers, see also [Disease, von Willebrand]D68.022

defective von Willebrand factor to factor VIII binding, see also [Disease, von Willebrand]D68.023

high-molecular-weight von Willebrand factor loss, see also [Disease, von Willebrand]D68.021

hyper-adhesive forms, see also [Disease, von Willebrand]D68.021

increased affinity for platelet glycoprotein lb, see also [Disease, von Willebrand]D68.021

markedly decreased affinity for factor VIII, see also [Disease, von Willebrand]D68.023

in von Willebrand factor function, with no further subtyping, see also [Disease, von Willebrand]D68.029

reduction

limbQ73.8

lowerQ72.9-

absence, see [Agenesis, leg]

foot, see [Agenesis, foot]

longitudinal

femurQ72.4-

fibulaQ72.6-

tibiaQ72.5-

specified type NECQ72.89-

split footQ72.7-

specified type NECQ73.8

upperQ71.9-

absence, see [Agenesis, arm]

forearm, see [Agenesis, forearm]

hand, see [Agenesis, hand]

lobster-claw handQ71.6-

longitudinal

radiusQ71.4-

ulnaQ71.5-

specified type NECQ71.89-

renal pelvisQ63.8

obstructiveQ62.39

respiratory system, congenitalQ34.9

restoration, dentalK08.50

specified NECK08.59

retinal nerve bundle fibersH35.89

septal NOSQ21.9

acquired I51.0

atrial, see also [Defect, atrial septal]Q21.10

concurrent with acute myocardial infarction, see [Infarct, myocardium]

following acute myocardial infarction I23.1

ventricular, see also [Defect, ventricular septal]Q21.0

sinus venosus, see also [Defect, atrial septal, sinus venosus]Q21.16

speech, see [Disorder, speech]

developmentalF80.9

specified NECR47.89

Taussig-Bing Q20.1

teeth, wedgeK03.1

vascular I99.9

congenitalQ27.9

ventricular septalQ21.0

concurrent with acute myocardial infarction, see [Infarct, myocardium]

following acute myocardial infarction I23.2

in tetralogy of FallotQ21.3

vision NECH54.7

visual fieldH53.40

bilateral

heteronymousH53.47

homonymousH53.46-

generalized contractionH53.48-

localized

arcuateH53.43-

scotoma H53.41-

blind spot areaH53.42-

sectorH53.43-

specified type NECH53.45-

voiceR49.9

specified NECR49.8

wedge, tooth, teeth K03.1