Defect, defective

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

Q21.10

coronary sinus

Q21.13

following acute myocardial infarction(current complication)

I23.1

ostium primum type(type I)

Q21.20

with

common atrioventricular valves and moderate or larger inlet VSD

Q21.23

separate atrioventricular valves

Q21.21

and small or restrictive inlet VSD

Q21.22

ostium secundum type(patent persistent) (type II)

Q21.11

sinus venosus

Q21.16

inferior

Q21.15

superior

Q21.14

specified NEC

Q21.19

vena cava type

inferior

Q21.15

superior

Q21.14

atrioventricular

canal

Q21.20

septal

common

Q21.23

complete

Q21.23

incomplete

Q21.21

intermediate

Q21.22

partial

Q21.21

transitional

Q21.22

unspecified as to partial or complete

Q21.20

septum

Q21.20

auricular septal

Q21.10

bilirubin excretion NEC

E80.6

biosynthesis, androgen(testicular)

E29.1

bulbar septum

Q21.0

catalase

E80.3

cell membrane receptor complex(CR3)

D71.8

circulation

I99.9

congenital

Q28.9

newborn

Q28.9

coagulation(factor)

D68.9

See also: Deficiency, factor

with

COVID-19 associated coagulopathy

D68.8

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

Q21.13

cushion, endocardial

Q21.20

common

Q21.23

incomplete

Q21.21

intermediate

Q21.22

transitional

Q21.22

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(gamma aminobutyric acid) metabolic

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

home, technical, preventing adequate care

Z59.19

interatrial septal

Q21.19

interauricular septal

Q21.19

interventricular septal

Q21.0

with dextroposition of aorta, pulmonary stenosis and hypertrophy of right ventricle

Q21.3

in tetralogy of Fallot

Q21.3

intervertebral annular fibrosis

M51.9

See also: Disease, intervertebral disc, by site

lumbar

M51.A0

large

M51.A2

small

M51.A1

lumbosacral

M51.A3

large

M51.A5

small

M51.A4

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

primum

Q21.20

secundum

Q21.11

peroxidase

E80.3

placental blood supply

See: Insufficiency, placental

platelets, qualitative

D69.19

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

D68.020

See also: Disease, von Willebrand

defective platelet adhesion with a normal size distribution of von Willebrand factor multimers

D68.022

See also: Disease, von Willebrand

defective von Willebrand factor to factor VIII binding

D68.023

See also: Disease, von Willebrand

high-molecular-weight von Willebrand factor loss

D68.021

See also: Disease, von Willebrand

hyper-adhesive forms

D68.021

See also: Disease, von Willebrand

increased affinity for platelet glycoprotein lb

D68.021

See also: Disease, von Willebrand

markedly decreased affinity for factor VIII

D68.023

See also: Disease, von Willebrand

in von Willebrand factor function, with no further subtyping

D68.029

See also: Disease, von Willebrand