Alphabetic Index | Tabular List | Neoplasms | Drugs and Chemicals | Injuries
Cystadenocarcinoma
Neoplasm, malignant, by site
bile duct
C22.1
endometrioid
Neoplasm, malignant, by site
specified site
Neoplasm, malignant, by site
unspecified site
female
C56.9
male
C61
mucinous
papillary
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
papillary
mucinous
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
pseudomucinous
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
serous
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
pseudomucinous
papillary
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
serous
papillary
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
specified site
Neoplasm, malignant, by site
unspecified site
C56.9
Cystadenofibroma
clear cell
Neoplasm, benign, by site
endometrioid
D27.9
borderline malignancy
D39.1-
malignant
C56.-
mucinous
specified site
Neoplasm, benign, by site
unspecified site
D27.9
serous
specified site
Neoplasm, benign, by site
unspecified site
D27.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
Cystadenoma
Neoplasm, benign, by site
bile duct
D13.4
endometrioid
Neoplasm, benign, by site
borderline malignancy
Neoplasm, uncertain behavior, by site
malignant
Neoplasm, malignant, by site
mucinous
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
papillary
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
papillary
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
lymphomatosum
specified site
Neoplasm, benign, by site
unspecified site
D11.9
mucinous
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
pseudomucinous
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
serous
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
pseudomucinous
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
papillary
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
serous
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
papillary
borderline malignancy
ovary
C56.-
specified site NEC
Neoplasm, uncertain behavior, by site
unspecified site
C56.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
specified site
Neoplasm, benign, by site
unspecified site
D27.9
Cystathionine synthase deficiency
E72.11
Cystathioninemia
E72.19
Cystathioninuria
E72.19
Cystic
condition
breast
(chronic)
Mastopathy, cystic
corpora lutea
(hemorrhagic)
N83.1-
duct
condition
eyeball
(congenital)
Q11.0
fibrosis
Fibrosis, cystic
kidney
(congenital)
Q61.9
adult type
Q61.2
infantile type NEC
Q61.19
collecting duct dilatation
Q61.11
medullary
Q61.5
liver, congenital
Q44.6
lung disease
J98.4
congenital
Q33.0
mastitis, chronic
Mastopathy, cystic
medullary, kidney
Q61.5
meniscus
Derangement, knee, meniscus, cystic
ovary
N83.20-
Cysticercosis, cysticerciasis
B69.9
with
epileptiform fits
B69.0
myositis
B69.81
brain
B69.0
central nervous system
B69.0
cerebral
B69.0
ocular
B69.1
specified NEC
B69.89
Cysticercus cellulose infestation
Cysticercosis
Cystinosis
(malignant)
E72.04
Cystinuria
E72.01
Cystitis
(exudative) (hemorrhagic) (septic) (suppurative)
N30.90
with
fibrosis
Cystitis, chronic, interstitial
hematuria
N30.91
leukoplakia
Cystitis, chronic, interstitial
malakoplakia
Cystitis, chronic, interstitial
metaplasia
Cystitis, chronic, interstitial
prostatitis
N41.3
acute
N30.00
with hematuria
N30.01
of trigone
N30.30
with hematuria
N30.31
allergic
Cystitis, specified type NEC
amebic
A06.81
bilharzial
B65.9
N33
blennorrhagic
(gonococcal)
A54.01
bullous
Cystitis, specified type NEC
calculous
N21.0
chlamydial
A56.01
chronic
N30.20
with hematuria
N30.21
interstitial
N30.10
with hematuria
N30.11
of trigone
N30.30
with hematuria
N30.31
specified NEC
N30.20
with hematuria
N30.21
cystic
(a)
Cystitis, specified type NEC
diphtheritic
A36.85
echinococcal
granulosus
B67.39
multilocularis
B67.69
emphysematous
Cystitis, specified type NEC
encysted
Cystitis, specified type NEC
eosinophilic
Cystitis, specified type NEC
follicular
Cystitis, of trigone
gangrenous
Cystitis, specified type NEC
glandularis
Cystitis, specified type NEC
gonococcal
A54.01
incrusted
Cystitis, specified type NEC
interstitial
(chronic)
Cystitis, chronic, interstitial
irradiation
N30.40
with hematuria
N30.41
irritation
Cystitis, specified type NEC
malignant
Cystitis, specified type NEC
of trigone
N30.30
with hematuria
N30.31
panmural
Cystitis, chronic, interstitial
polyposa
Cystitis, specified type NEC
prostatic
N41.3
puerperal
(postpartum)
O86.22
radiation
Cystitis, irradiation
specified type NEC
N30.80
with hematuria
N30.81
subacute
Cystitis, chronic
submucous
Cystitis, chronic, interstitial
syphilitic
(late)
A52.76
trichomonal
A59.03
tuberculous
A18.12
ulcerative
Cystitis, chronic, interstitial
Cystocele
(-urethrocele)
female
N81.10
with prolapse of uterus
Prolapse, uterus
lateral
N81.12
midline
N81.11
paravaginal
N81.12
in pregnancy or childbirth
O34.8-
causing obstructed labor
O65.5
male
N32.89
Cystolithiasis
N21.0
Cystoma
Neoplasm, benign, by site
endometrial, ovary
N80.1
mucinous
specified site
Neoplasm, benign, by site
unspecified site
D27.9
serous
specified site
Neoplasm, benign, by site
unspecified site
D27.9
simple
(ovary)
N83.29-
Cystoplegia
N31.2
Cystoptosis
N32.89
Cystopyelitis
Pyelonephritis
Cystorrhagia
N32.89
Cystosarcoma phyllodes
D48.6-
benign
D24-
malignant
Neoplasm, breast, malignant
Cystostomy
attention to
Z43.5
complication
Complications, cystostomy
status
Z93.50
appendico-vesicostomy
Z93.52
cutaneous
Z93.51
specified NEC
Z93.59
Cystourethritis
Urethritis
Cystourethrocele
Cystocele
female
N81.10
with uterine prolapse
Prolapse, uterus
lateral
N81.12
midline
N81.11
paravaginal
N81.12
male
N32.89
Cytomegalic inclusion disease
congenital
P35.1
Cytomegalovirus infection
B25.9
Cytomycosis
(reticuloendothelial)
B39.4
Cytopenia
D75.9
refractory
with multilineage dysplasia
D46.A
and ring sideroblasts
(RCMD RS)
D46.B
Czerny's disease
(periodic hydrarthrosis of the knee)
Effusion, joint, knee
Daae
(-Finsen) disease (epidemic pleurodynia)
B33.0
Da Costa's syndrome
F45.8
Dabney's grip
B33.0
Dacryoadenitis, dacryadenitis
H04.00-
acute
H04.01-
chronic
H04.02-
Dacryocystitis
H04.30-
acute
H04.32-
chronic
H04.41-
neonatal
P39.1
phlegmonous
H04.31-
syphilitic
A52.71
congenital
(early)
A50.01
trachomatous, active
A71.1
sequelae
(late effect)
B94.0
Dacryocystoblenorrhea
Inflammation, lacrimal, passages, chronic
Dacryocystocele
Disorder, lacrimal system, changes
Dacryolith, dacryolithiasis
H04.51-
Dacryoma
Disorder, lacrimal system, changes
Dacryopericystitis
Dacryocystitis
Dacryops
H04.11-
Dacryostenosis
Stenosis, lacrimal
congenital
Q10.5
Dactylitis
bone
Osteomyelitis
sickle-cell
D57.00
Hb C
D57.219
Hb SS
D57.00
specified NEC
D57.819
skin
L08.9
syphilitic
A52.77
tuberculous
A18.03
Dactylolysis spontanea
(ainhum)
L94.6
Dactylosymphysis
Q70.9
fingers
Syndactylism, complex, fingers
toes
Syndactylism, complex, toes
Damage
arteriosclerotic
Arteriosclerosis
brain
(nontraumatic)
G93.9
anoxic, hypoxic
G93.1
resulting from a procedure
G97.82
child NEC
G80.9
due to birth injury
P11.2
cardiorenal
(vascular)
Hypertension, cardiorenal
cerebral NEC
Damage, brain
coccyx, complicating delivery
O71.6
coronary
Disease, heart, ischemic
eye, birth injury
P15.3
liver
(nontraumatic)
K76.9
alcoholic
K70.9
due to drugs
Disease, liver, toxic
toxic
Disease, liver, toxic
medication
T88.7
pelvic
joint or ligament, during delivery
O71.6
organ NEC
during delivery
O71.5
following ectopic or molar pregnancy
O08.6
renal
Disease, renal
subendocardium, subendocardial
Degeneration, myocardial
vascular
I99.9
Dana-Putnam syndrome
(subacute combined sclerosis with pernicious anemia)
Degeneration, combined
Danbolt
(-Cross) syndrome (acrodermatitis enteropathica)
E83.2
Dandruff
L21.0
Dandy-Walker syndrome
Q03.1
with spina bifida
Spina bifida
Danlos' syndrome
Q79.6
Darier
(-White) disease (congenital)
Q82.8
meaning erythema annulare centrifugum
L53.1
Darier-Roussy sarcoid
D86.3
Darling's disease or histoplasmosis
B39.4
Darwin's tubercle
Q17.8
Dawson's encephalitis
(inclusion body)
A81.1
De Beurmann disease
(-Gougerot)
B42.1
De la Tourette's syndrome
F95.2
De Lange's syndrome
Q87.1
De Morgan's spots
(senile angiomas)
I78.1
De Quervain's
disease
(tendon sheath)
M65.4
syndrome
E34.51
thyroiditis
(subacute granulomatous thyroiditis)
E06.1
De Toni-Fanconi syndrome
(-Debré)
E72.09
with cystinosis
E72.04
Dead
fetus, retained
(mother)
O36.4
early pregnancy
O02.1
labyrinth
H83.2
ovum, retained
O02.0
Deaf nonspeaking NEC
H91.3
Deafmutism NEC
(acquired) (congenital)
H91.3
hysterical
F44.6
syphilitic, congenital
A50.09
subcategory H94.8
Deafness
(acquired) (complete) (hereditary) (partial)
H91.9-
with blue sclera and fragility of bone
Q78.0
auditory fatigue
Deafness, specified type NEC
aviation
T70.0
nerve injury
Injury, nerve, acoustic, specified type NEC
boilermaker's
H83.3
central
Deafness, sensorineural
conductive
H90.2
and sensorineural
mixed
H90.8
bilateral
H90.6
bilateral
H90.0
unilateral
H90.1-
with restricted hearing on the contralateral side
H90.A-
congenital
H90.5
with blue sclera and fragility of bone
Q78.0
due to toxic agents
Deafness, ototoxic
emotional
(hysterical)
F44.6
functional
(hysterical)
F44.6
high frequency
H91.9-
hysterical
F44.6
low frequency
H91.9-
mental
R48.8
mixed conductive and sensorineural
H90.8
bilateral
H90.6
unilateral
H90.7-
nerve
Deafness, sensorineural
neural
Deafness, sensorineural
noise-induced
H83.3
subcategory
nerve injury
Injury, nerve, acoustic, specified type NEC
nonspeaking
H91.3
ototoxic
H91.0
perceptive
Deafness, sensorineural
psychogenic
(hysterical)
F44.6
sensorineural
H90.5
and conductive
mixed
H90.8
bilateral
H90.6
bilateral
H90.3
unilateral
H90.4-
with restricted hearing on the contralateral side
H90.A-
sensory
Deafness, sensorineural
specified type NEC
H91.8
sudden
(idiopathic)
H91.2-
syphilitic
A52.15
transient ischemic
H93.01-
traumatic
Injury, nerve, acoustic, specified type NEC
word
(developmental)
H93.25
Death
(cause unknown) (of) (unexplained) (unspecified cause)
R99
brain
G93.82
cardiac - code to underlying disease
(sudden) (with successful resuscitation)
family history of
Z82.41
personal history of
Z86.74
family member
(assumed)
Z63.4
Debility
(chronic) (general) (nervous)
R53.81
congenital or neonatal NOS
P96.9
nervous
R53.81
old age
R54
senile
R54
Débove's disease
(splenomegaly)
R16.1
Decalcification
bone
Osteoporosis
teeth
K03.89
Decapsulation, kidney
N28.89
Decay
dental
Caries, dental
senile
R54
tooth, teeth
Caries, dental
Deciduitis
(acute)
following ectopic or molar pregnancy
O08.0
Decline
(general)
Debility
cognitive, age-associated
R41.81
Decompensation
cardiac
(acute) (chronic)
Disease, heart
cardiovascular
Disease, cardiovascular
heart
Disease, heart
hepatic
Failure, hepatic
myocardial
(acute) (chronic)
Disease, heart
respiratory
J98.8
Decompression sickness
T70.3
Decrease
(d)
absolute neutrophile count
Neutropenia
blood
platelets
Thrombocytopenia
pressure
R03.1
due to shock following
injury
T79.4
operation
T81.19
estrogen
E28.39
postablative
E89.40
asymptomatic
E89.40
symptomatic
E89.41
fragility of erythrocytes
D58.8
function
lipase
(pancreatic)
K90.3
ovary in hypopituitarism
E23.0
parenchyma of pancreas
K86.89
pituitary
(gland) (anterior) (lobe)
E23.0
posterior
(lobe)
E23.0
functional activity
R68.89
glucose
R73.09
hematocrit
R71.0
hemoglobin
R71.0
leukocytes
D72.819
specified NEC
D72.818
libido
R68.82
lymphocytes
D72.810
platelets
D69.6
respiration, due to shock following injury
T79.4
sexual desire
R68.82
tear secretion NEC
Syndrome, dry eye
tolerance
fat
K90.49
glucose
R73.09
pancreatic
K90.3
salt and water
E87.8
vision NEC
H54.7
white blood cell count
D72.819
specified NEC
D72.818
Decubitus
(ulcer)
Ulcer, pressure, by site
cervix
N86
Deepening acetabulum
Derangement, joint, specified type NEC, hip
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)
D68.9
Deficiency, factor
with
ectopic pregnancy
O08.1
molar pregnancy
O08.1
acquired
D68.4
antepartum with hemorrhage
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
Deafness, conductive
congenital, organ or site not listed
Anomaly, by site
coronary sinus
Q21.1
cushion, endocardial
Q21.2
degradation, glycoprotein
E77.1
dental bridge, crown, fillings
Defect, dental restoration
dental restoration
K08.50
specified NEC
K08.59
dentin
(hereditary)
K00.5
Descemet's membrane, congenital
Q13.89
developmental
Anomaly
cauda equina
Q06.3
diaphragm
with elevation, eventration or hernia
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
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)
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
Disability, intellectual
modification, lysosomal enzymes, post-translational
E77.0
obstructive, congenital
renal pelvis
Q62.39
ureter
Q62.39
atresia
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
Deformity
ostium
primum
Q21.2
secundum
Q21.1
peroxidase
E80.3
placental blood supply
Insufficiency, placental
platelets, qualitative
D69.1
constitutional
D68.0
postural NEC, spine
Dorsopathy, deforming
reduction
limb
Q73.8
lower
Q72.9-
absence
Agenesis, leg
foot
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
Agenesis, arm
forearm
Agenesis, forearm
hand
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
Infarct, myocardium
following acute myocardial infarction
(current complication)
I23.1
ventricular
Q21.0
Defect, ventricular septal
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
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
Deferentitis
N49.1
gonorrheal
(acute) (chronic)
A54.23
Defibrination
(syndrome)
D65
antepartum
Hemorrhage, antepartum, with coagulation defect, disseminated intravascular coagulation
following ectopic or molar pregnancy
O08.1
intrapartum
O67.0
newborn
P60
postpartum
O72.3
Deficiency, deficient
3-beta hydroxysteroid dehydrogenase
E25.0
5-alpha reductase
(with male pseudohermaphroditism)
E29.1
11-hydroxylase
E25.0
21-hydroxylase
E25.0
abdominal muscle syndrome
Q79.4
accelerator globulin
(Ac G) (blood)
D68.2
AC globulin
(congenital) (hereditary)
D68.2
acquired
D68.4
acid phosphatase
E83.39
activating factor
(blood)
D68.2
adenosine deaminase
(ADA)
D81.3
aldolase
(hereditary)
E74.19
alpha-1-antitrypsin
E88.01
amino-acids
E72.9
anemia
Anemia
aneurin
E51.9
antibody with
hyperimmunoglobulinemia
D80.6
near-normal immunoglobins
D80.6
antidiuretic hormone
E23.2
anti-hemophilic
factor
(A)
D66
B
D67
C
D68.1
globulin NEC
(AHG)
D66
antithrombin
(antithrombin III)
D68.59
ascorbic acid
E54
attention
(disorder) (syndrome)
F98.8
with hyperactivity
Disorder, attention-deficit hyperactivity
autoprothrombin
I
D68.2
II
D67
C
D68.2
beta-glucuronidase
E76.29
biotin
E53.8
biotin-dependent carboxylase
D81.819
biotinidase
D81.810
brancher enzyme
(amylopectinosis)
E74.03
calciferol
E55.9
with
adult osteomalacia
M83.8
rickets
Rickets
calcium
(dietary)
E58
calorie, severe
E43
with marasmus
E41
and kwashiorkor
E42
cardiac
Insufficiency, myocardial
carnitine
E71.40
due to
hemodialysis
E71.43
inborn errors of metabolism
E71.42
Valproic acid therapy
E71.43
iatrogenic
E71.43
muscle palmityltransferase
E71.314
primary
E71.41
secondary
E71.448
carotene
E50.9
central nervous system
G96.8
ceruloplasmin
(Wilson)
E83.01
choline
E53.8
Christmas factor
D67
chromium
E61.4
clotting
(blood)
D68.9
Deficiency, coagulation factor
clotting factor NEC
(hereditary)
D68.2
Deficiency, factor
coagulation NOS
D68.9
with
ectopic pregnancy
O08.1
molar pregnancy
O08.1
acquired
(any)
D68.4
antepartum hemorrhage
Hemorrhage, antepartum, with coagulation defect
clotting factor NEC
D68.2
Deficiency, factor
due to
hyperprothrombinemia
D68.4
liver disease
D68.4
vitamin K deficiency
D68.4
newborn, transient
P61.6
postpartum
O72.3
specified NEC
D68.8
cognitive
F09
color vision
H53.50
achromatopsia
H53.51
acquired
H53.52
deuteranomaly
H53.53
protanomaly
H53.54
specified type NEC
H53.59
tritanomaly
H53.55
combined glucocorticoid and mineralocorticoid
E27.49
contact factor
D68.2
copper
(nutritional)
E61.0
corticoadrenal
E27.40
primary
E27.1
craniofacial axis
Q75.0
cyanocobalamin
E53.8
C1 esterase inhibitor
(C1-INH)
D84.1
debrancher enzyme
(limit dextrinosis)
E74.03
dehydrogenase
long chain/very long chain acyl CoA
E71.310
medium chain acyl CoA
E71.311
short chain acyl CoA
E71.312
diet
E63.9
dihydropyrimidine dehydrogenase
(DPD)
E88.89
disaccharidase
E73.9
edema
Malnutrition, severe
endocrine
E34.9
energy-supply
Malnutrition
enzymes, circulating NEC
E88.09
ergosterol
E55.9
with
adult osteomalacia
M83.8
rickets
Rickets
essential fatty acid
(EFA)
E63.0
factor
Deficiency, coagulation
Hageman
D68.2
I
(congenital) (hereditary)
D68.2
II
(congenital) (hereditary)
D68.2
IX
(congenital) (functional) (hereditary) (with functional defect)
D67
multiple
(congenital)
D68.8
acquired
D68.4
V
(congenital) (hereditary)
D68.2
VII
(congenital) (hereditary)
D68.2
VIII
(congenital) (functional) (hereditary) (with functional defect)
D66
with vascular defect
D68.0
X
(congenital) (hereditary)
D68.2
XI
(congenital) (hereditary)
D68.1
XII
(congenital) (hereditary)
D68.2
XIII
(congenital) (hereditary)
D68.2
femoral, proximal focal
(congenital)
Defect, reduction, lower limb, longitudinal, femur
fibrin-stabilizing factor
(congenital) (hereditary)
D68.2
acquired
D68.4
fibrinase
D68.2
fibrinogen
(congenital) (hereditary)
D68.2
acquired
D65
folate
E53.8
folic acid
E53.8
foreskin
N47.3
fructokinase
E74.11
fructose 1,6-diphosphatase
E74.19
fructose-1-phosphate aldolase
E74.19
GABA transaminase
(gamma aminobutyric acid)
E72.81
GABA-T
(gamma aminobutyric acid transaminase)
E72.81
galactokinase
E74.29
galactose-1-phosphate uridyl transferase
E74.29
gammaglobulin in blood
D80.1
hereditary
D80.0
glass factor
D68.2
glucocorticoid
E27.49
mineralocorticoid
E27.49
glucose-6-phosphatase
E74.01
glucose-6-phosphate dehydrogenase anemia
D55.0
glucuronyl transferase
E80.5
glycogen synthetase
E74.09
gonadotropin
(isolated)
E23.0
growth hormone
(idiopathic) (isolated)
E23.0
Hageman factor
D68.2
hemoglobin
D64.9
hepatophosphorylase
E74.09
homogentisate 1,2-dioxygenase
E70.29
hormone
anterior pituitary NEC
(partial)
E23.0
growth
E23.0
growth
(isolated)
E23.0
pituitary
E23.0
testicular
E29.1
hypoxanthine-
(guanine)-phosphoribosyltransferase (HG- PRT) (total H-PRT)
E79.1
immunity
D84.9
cell-mediated
D84.8
with thrombocytopenia and eczema
D82.0
combined
D81.9
humoral
D80.9
IgA
(secretory)
D80.2
IgG
D80.3
IgM
D80.4
immuno
Immunodeficiency
immunoglobulin, selective
A
(IgA)
D80.2
G
(IgG) (subclasses)
D80.3
M
(IgM)
D80.4
inositol
(B complex)
E53.8
intrinsic
factor
(congenital)
D51.0
sphincter
N36.42
with urethral hypermobility
N36.43
iodine
E61.8
congenital syndrome
Syndrome, iodine-deficiency, congenital
iron
E61.1
anemia
D50.9
kalium
E87.6
kappa-light chain
D80.8
labile factor
(congenital) (hereditary)
D68.2
acquired
D68.4
lacrimal fluid
(acquired)
Syndrome, dry eye
congenital
Q10.6
lactase
congenital
E73.0
secondary
E73.1
Laki-Lorand factor
D68.2
lecithin cholesterol acyltransferase
E78.6
lipocaic
K86.89
lipoprotein
(familial) (high density)
E78.6
liver phosphorylase
E74.09
lysosomal alpha-1, 4 glucosidase
E74.02
magnesium
E61.2
major histocompatibility complex
class I
D81.6
class II
D81.7
manganese
E61.3
menadione
(vitamin K)
E56.1
newborn
P53
mental
(familial) (hereditary)
Disability, intellectual
methylenetetrahydrofolate reductase
(MTHFR)
E72.12
mevalonate kinase
M04.1
mineral NEC
E61.8
mineralocorticoid
E27.49
with glucocorticoid
E27.49
molybdenum
(nutritional)
E61.5
moral
F60.2
multiple nutrient elements
E61.7
multiple sulfatase
(MSD)
E75.26
muscle
carnitine
(palmityltransferase)
E71.314
phosphofructokinase
E74.09
myoadenylate deaminase
E79.2
myocardial
Insufficiency, myocardial
myophosphorylase
E74.04
NADH diaphorase or reductase
(congenital)
D74.0
NADH-methemoglobin reductase
(congenital)
D74.0
natrium
E87.1
niacin
(amide) (-tryptophan)
E52
nicotinamide
E52
nicotinic acid
E52
number of teeth
Anodontia
nutrient element
E61.9
multiple
E61.7
specified NEC
E61.8
nutrition, nutritional
E63.9
sequelae
Sequelae, nutritional deficiency
specified NEC
E63.8
of interleukin 1 receptor antagonist [DIRA]
M04.8
ornithine transcarbamylase
E72.4
ovarian
E28.39
oxygen
Anoxia
pantothenic acid
E53.8
parathyroid
(gland)
E20.9
perineum
(female)
N81.89
phenylalanine hydroxylase
E70.1
phosphoenolpyruvate carboxykinase
E74.4
phosphofructokinase
E74.19
phosphomannomutuse
E74.8
phosphomannose isomerase
E74.8
phosphomannosyl mutase
E74.8
phosphorylase kinase, liver
E74.09
pituitary hormone
(isolated)
E23.0
plasma thromboplastin
antecedent
(PTA)
D68.1
component
(PTC)
D67
plasminogen
(type 1) (type 2)
E88.02
platelet NEC
D69.1
constitutional
D68.0
polyglandular
E31.8
autoimmune
E31.0
potassium
(K)
E87.6
prepuce
N47.3
proaccelerin
(congenital) (hereditary)
D68.2
acquired
D68.4
proconvertin factor
(congenital) (hereditary)
D68.2
acquired
D68.4
protein
E46
Malnutrition
anemia
D53.0
C
D68.59
S
D68.59
prothrombin
(congenital) (heredItary)
D68.2
acquired
D68.4
Prower factor
D68.2
pseudocholinesterase
E88.09
PTA
(plasma thromboplastin antecedent)
D68.1
PTC
(plasma thromboplastin component)
D67
purine nucleoside phosphorylase
(PNP)
D81.5
pyracin
(alpha) (beta)
E53.1
pyridoxal
E53.1
pyridoxamine
E53.1
pyridoxine
(derivatives)
E53.1
pyruvate
carboxylase
E74.4
dehydrogenase
E74.4
riboflavin
(vitamin B2)
E53.0
salt
E87.1
secretion
ovary
E28.39
salivary gland
(any)
K11.7
urine
R34
selenium
(dietary)
E59
serum antitrypsin, familial
E88.01
short stature homeobox gene
(SHOX)
with
dyschondrosteosis
Q78.8
short stature
(idiopathic)
E34.3
Turner's syndrome
Q96.9
sodium
(Na)
E87.1
SPCA
(factor VII)
D68.2
sphincter, intrinsic
N36.42
with urethral hypermobility
N36.43
stable factor
(congenital) (hereditary)
D68.2
acquired
D68.4
Stuart-Prower
(factor X)
D68.2
succinic semialdehyde dehydrogenase
E72.81
sucrase
E74.39
sulfatase
E75.26
sulfite oxidase
E72.19
thiamin, thiaminic
(chloride)
E51.9
beriberi
(dry)
E51.11
wet
E51.12
thrombokinase
D68.2
newborn
P53
thyroid
(gland)
Hypothyroidism
tocopherol
E56.0
tooth bud
K00.0
transcobalamine II
(anemia)
D51.2
vanadium
E61.6
vascular
I99.9
vasopressin
E23.2
vertical ridge
K06.8
viosterol
Deficiency, calciferol
vitamin NOS
(multiple)
E56.9
A
E50.9
with
Bitot's spot
(corneal)
E50.1
follicular keratosis
E50.8
keratomalacia
E50.4
manifestations NEC
E50.8
night blindness
E50.5
scar of cornea, xerophthalmic
E50.6
xeroderma
E50.8
xerophthalmia
E50.7
xerosis
conjunctival
E50.0
and Bitot's spot
E50.1
cornea
E50.2
and ulceration
E50.3
sequelae
E64.1
B NOS
(complex)
E53.9
with
beriberi
(dry)
E51.11
wet
E51.12
pellagra
E52
B1 NOS
E51.9
beriberi
(dry)
E51.11
with circulatory system manifestations
E51.11
wet
E51.12
B12
E53.8
B2
(riboflavin)
E53.0
B6
E53.1
C
E54
sequelae
E64.2
D
E55.9
with
adult osteomalacia
M83.8
rickets
Rickets
25-hydroxylase
E83.32
E
E56.0
folic acid
E53.8
G
E53.0
group B
E53.9
specified NEC
E53.8
H
(biotin)
E53.8
K
E56.1
of newborn
P53
nicotinic
E52
P
E56.8
PP
(pellagra-preventing)
E52
specified NEC
E56.8
thiamin
E51.9
beriberi
Beriberi
zinc, dietary
E60
Deficit
Deficiency
attention and concentration
R41.840
following
cerebral infarction
I69.310
cerebrovascular disease
I69.910
specified disease NEC
I69.810
nontraumatic
intracerebral hemorrhage
I69.110
specified intracranial hemorrhage NEC
I69.210
subarachnoid hemorrhage
I69.010
disorder
Attention, deficit
cognitive
communication
R41.841
emotional
following
cerebral infarction
I69.315
cerebrovascular disease
I69.915
specified disease NEC
I69.815
nontraumatic
intracerebral hemorrhage
I69.115
specified intracranial hemorrhage NEC
I69.215
subarachnoid hemorrhage
I69.015
following
cerebral infarction
I69.319
cerebrovascular disease
I69.919
specified disease NEC
I69.819
nontraumatic
intracerebral hemorrhage
I69.119
specified intracranial hemorrhage NEC
I69.219
subarachnoid hemorrhage
I69.019
social
following
cerebral infarction
I69.315
cerebrovascular disease
I69.915
specified disease NEC
I69.815
nontraumatic
intracerebral hemorrhage
I69.115
specified intracranial hemorrhage NEC
I69.215
subarachnoid hemorrhage
I69.015
cognitive NEC
R41.89
following
cerebral infarction
I69.318
cerebrovascular disease
I69.918
specified disease NEC
I69.818
nontraumatic
intracerebral hemorrhage
I69.118
specified intracranial hemorrhage NEC
I69.218
subarachnoid hemorrhage
I69.018
concentration
R41.840
executive function
R41.844
following
cerebral infarction
I69.314
cerebrovascular disease
I69.914
specified disease NEC
I69.814
nontraumatic
intracerebral hemorrhage
I69.114
specified intracranial hemorrhage NEC
I69.214
subarachnoid hemorrhage
I69.014
frontal lobe
R41.844
following
cerebral infarction
I69.314
cerebrovascular disease
I69.914
specified disease NEC
I69.814
nontraumatic
intracerebral hemorrhage
I69.114
specified intracranial hemorrhage NEC
I69.214
subarachnoid hemorrhage
I69.014
memory
following
cerebral infarction
I69.311
cerebrovascular disease
I69.911
specified disease NEC
I69.811
nontraumatic
intracerebral hemorrhage
I69.111
specified intracranial hemorrhage NEC
I69.211
subarachnoid hemorrhage
I69.011
neurologic NEC
R29.818
ischemic
reversible
(RIND)
I63.9
prolonged
(PRIND)
I63.9
oxygen
R09.02
prolonged reversible ischemic neurologic
(PRIND)
I63.9
psychomotor
R41.843
following
cerebral infarction
I69.313
cerebrovascular disease
I69.913
specified disease NEC
I69.813
nontraumatic
intracerebral hemorrhage
I69.113
specified intracranial hemorrhage NEC
I69.213
subarachnoid hemorrhage
I69.013
visuospatial
R41.842
following
cerebral infarction
I69.312
cerebrovascular disease
I69.912
specified disease NEC
I69.812
nontraumatic
intracerebral hemorrhage
I69.112
specified intracranial hemorrhage NEC
I69.212
subarachnoid hemorrhage
I69.012
Deflection
radius
Deformity, limb, specified type NEC, forearm
septum
(acquired) (nasal) (nose)
J34.2
spine
Curvature, spine
turbinate
(nose)
J34.2
Defluvium
capillorum
Alopecia
ciliorum
Madarosis
unguium
L60.8
Deformity
Q89.9
abdomen, congenital
Q89.9
abdominal wall
acquired
M95.8
congenital
Q79.59
acquired
(unspecified site)
M95.9
adrenal gland
Q89.1
alimentary tract, congenital
Q45.9
upper
Q40.9
ankle
(joint) (acquired)
Deformity, limb, lower leg
abduction
Contraction, joint, ankle
congenital
Q68.8
contraction
Contraction, joint, ankle
specified type NEC
Deformity, limb, foot, specified NEC
anus
(acquired)
K62.89
congenital
Q43.9
aorta
(arch) (congenital)
Q25.40
acquired
I77.89
aortic
arch, acquired
I77.89
cusp or valve
(congenital)
Q23.8
acquired
I35.8
Endocarditis, aortic
arm
(acquired) (upper)
Deformity, limb, upper arm
congenital
Q68.8
forearm
Deformity, limb, forearm
artery NOS
(congenital) (peripheral)
Q27.9
acquired
I77.89
coronary
(acquired)
I25.9
congenital
Q24.5
umbilical
Q27.0
atrial septal
Q21.1
auditory canal
(external) (congenital)
Malformation, ear, external
acquired
Disorder, ear, external, specified type NEC
auricle
ear
(congenital)
Malformation, ear, external
acquired
Disorder, pinna, deformity
back
Dorsopathy, deforming
bile duct
(common) (congenital) (hepatic)
Q44.5
acquired
K83.8
biliary duct or passage
(congenital)
Q44.5
acquired
K83.8
bladder
(neck) (trigone) (sphincter) (acquired)
N32.89
congenital
Q64.79
bone NOS
(acquired)
M95.9
congenital
Q79.9
turbinate
M95.0
brain
(congenital)
Q04.9
acquired
G93.89
reduction
Q04.3
breast
(acquired)
N64.89
congenital
Q83.9
reconstructed
N65.0
bronchus
(congenital)
Q32.4
acquired NEC
J98.09
bursa, congenital
Q79.9
canaliculi
(lacrimalis) (acquired)
Disorder, lacrimal system, changes
congenital
Q10.6
canthus, acquired
Disorder, eyelid, specified type NEC
capillary
(acquired)
I78.8
cardiovascular system, congenital
Q28.9
caruncle, lacrimal
(acquired)
Disorder, lacrimal system, changes
congenital
Q10.6
cascade, stomach
K31.2
cecum
(congenital)
Q43.9
acquired
K63.89
cerebral, acquired
G93.89
congenital
Q04.9
cervix NEC
(uterus) (acquired)
N88.8
congenital
Q51.9
cheek
(acquired)
M95.2
congenital
Q18.9
chest
(acquired) (wall)
M95.4
congenital
Q67.8
sequelae of rickets
(late effect)
E64.3
chin
(acquired)
M95.2
congenital
Q18.9
choroid
(congenital)
Q14.3
acquired
H31.8
plexus
Q07.8
acquired
G96.19
cicatricial
Cicatrix
cilia, acquired
Disorder, eyelid, specified type NEC
clavicle
(acquired)
M95.8
congenital
Q68.8
clitoris
(congenital)
Q52.6
acquired
N90.89
clubfoot
Clubfoot
coccyx
(acquired)
M43.8
colon
(congenital)
Q43.9
acquired
K63.89
concha, congenital
(ear)
Malformation, ear, external
acquired
Disorder, pinna, deformity
cornea
(acquired)
H18.70
congenital
Q13.4
descemetocele
Descemetocele
ectasia
Ectasia, cornea
specified NEC
H18.79-
staphyloma
Staphyloma, cornea
coronary artery
(acquired)
I25.9
congenital
Q24.5
cranium
(acquired)
Deformity, skull
cricoid cartilage
(congenital)
Q31.8
acquired
J38.7
cystic duct
(congenital)
Q44.5
acquired
K82.8
Dandy-Walker
Q03.1
with spina bifida
Spina bifida
diaphragm
(congenital)
Q79.1
acquired
J98.6
digestive organ NOS
Q45.9
ductus arteriosus
Q25.0
duodenal bulb
K31.89
duodenum
(congenital)
Q43.9
acquired
K31.89
dura
Deformity, meninges
ear
(acquired)
Disorder, pinna, deformity
congenital
(external)
Q17.9
internal
Q16.5
middle
Q16.4
ossicles
Q16.3
ossicles
Q16.3
ectodermal NEC
(congenital)
Q84.9
ejaculatory duct
(congenital)
Q55.4
acquired
N50.89
elbow
(joint) (acquired)
Deformity, limb, upper arm
congenital
Q68.8
contraction
Contraction, joint, elbow
endocrine gland NEC
Q89.2
epididymis
(congenital)
Q55.4
acquired
N50.89
epiglottis
(congenital)
Q31.8
acquired
J38.7
esophagus
(congenital)
Q39.9
acquired
K22.8
eustachian tube NEC
(congenital)
Q17.8
eye, congenital
Q15.9
eyebrow
(congenital)
Q18.8
eyelid
(acquired)
Disorder, eyelid, specified type NEC
congenital
Q10.3
face
(acquired)
M95.2
congenital
Q18.9
fallopian tube, acquired
N83.8
femur
(acquired)
Deformity, limb, specified type NEC, thigh
fetal
with fetopelvic disproportion
O33.7
causing obstructed labor
O66.3
finger
(acquired)
M20.00-
boutonniere
M20.02-
congenital
Q68.1
flexion contracture
Contraction, joint, hand
mallet finger
M20.01-
specified NEC
M20.09-
swan-neck
M20.03-
flexion
(joint) (acquired)
M21.20
Deformity, limb, flexion
congenital NOS
Q74.9
hip
Q65.89
foot
(acquired)
Deformity, limb, lower leg
cavovarus
(congenital)
Q66.1
congenital NOS
Q66.9
specified type NEC
Q66.89
specified type NEC
Deformity, limb, foot, specified NEC
valgus
(congenital)
Q66.6
acquired
Deformity, valgus, ankle
varus NEC
(congenital)
Q66.3
acquired
Deformity, varus, ankle
forearm
(acquired)
Deformity, limb, forearm
congenital
Q68.8
forehead
(acquired)
M95.2
congenital
Q75.8
frontal bone
(acquired)
M95.2
congenital
Q75.8
gallbladder
(congenital)
Q44.1
acquired
K82.8
gastrointestinal tract NOS
(congenital)
Q45.9
acquired
K63.89
genitalia, genital organ or system NEC
(s)
female
(congenital)
Q52.9
acquired
N94.89
external
Q52.70
male
(congenital)
Q55.9
acquired
N50.89
globe
(eye) (congenital)
Q15.8
acquired
H44.89
gum, acquired NEC
K06.8
hand
(acquired)
Deformity, limb, hand
congenital
Q68.1
head
(acquired)
M95.2
congenital
Q75.8
heart
(congenital)
Q24.9
septum
Q21.9
auricular
Q21.1
ventricular
Q21.0
valve NEC
(congenital)
Q24.8
acquired
Endocarditis
heel
(acquired)
Deformity, foot
hepatic duct
(congenital)
Q44.5
acquired
K83.8
hip
(joint) (acquired)
Deformity, limb, thigh
congenital
Q65.9
due to juvenile osteochondrosis
(previous)
Coxa, plana
flexion
Contraction, joint, hip
hourglass
Contraction, hourglass
humerus
(acquired)
M21.82-
congenital
Q74.0
hypophyseal
(congenital)
Q89.2
ileocecal
(coil) (valve) (acquired)
K63.89
congenital
Q43.9
ileum
(congenital)
Q43.9
acquired
K63.89
ilium
(acquired)
M95.5
congenital
Q74.2
integument
(congenital)
Q84.9
intervertebral cartilage or disc
(acquired)
Disorder, disc, specified NEC
intestine NOS
(large) (small) (congenital)
Q43.9
acquired
K63.89
intrinsic minus or plus
(hand)
Deformity, limb, specified type NEC, forearm
iris
(acquired)
H21.89
congenital
Q13.2
ischium
(acquired)
M95.5
congenital
Q74.2
jaw
(acquired) (congenital)
M26.9
joint NEC
(acquired)
M21.90
congenital
Q68.8
elbow
M21.92-
hand
M21.94-
hip
M21.95-
knee
M21.96-
shoulder
M21.92-
wrist
M21.93-
kidney
(s) (calyx) (pelvis) (congenital)
Q63.9
acquired
N28.89
artery
(congenital)
Q27.2
acquired
I77.89
Klippel-Feil
(brevicollis)
Q76.1
knee NEC
(acquired)
Deformity, limb, lower leg
congenital
Q68.2
labium
(majus) (minus) (congenital)
Q52.79
acquired
N90.89
lacrimal passages or duct NEC
(congenital)
Q10.6
acquired
Disorder, lacrimal system, changes
larynx
(muscle) (congenital)
Q31.8
acquired
J38.7
web
(glottic)
Q31.0
leg NEC
(upper) (acquired)
Deformity, limb, thigh
congenital
Q68.8
lower leg
Deformity, limb, lower leg
lens
(acquired)
H27.8
congenital
Q12.9
lid
(fold) (acquired)
Disorder, eyelid, specified type NEC
congenital
Q10.3
ligament
(acquired)
Disorder, ligament
congenital
Q79.9
limb
(acquired)
M21.90
clawfoot
M21.53-
clawhand
M21.51-
clubfoot
M21.54-
clubhand
M21.52-
congenital, except reduction deformity
Q74.9
flat foot
M21.4-
flexion
M21.20
ankle
M21.27-
elbow
M21.22-
finger
M21.24-
hip
M21.25-
knee
M21.26-
shoulder
M21.21-
toe
M21.27-
wrist
M21.23-
foot
claw
Deformity, limb, clawfoot
club
Deformity, limb, clubfoot
drop
M21.37-
flat
Deformity, limb, flat foot
specified NEC
M21.6X-
forearm
M21.93-
hand
M21.94-
lower leg
M21.96-
specified type NEC
M21.80
forearm
M21.83-
lower leg
M21.86-
thigh
M21.85-
upper arm
M21.82-
thigh
M21.95-
unequal length
M21.70
short site is
femur
M21.75-
fibula
M21.76-
humerus
M21.72-
radius
M21.73-
tibia
M21.76-
ulna
M21.73-
upper arm
M21.92-
valgus
Deformity, valgus
varus
Deformity, varus
wrist drop
M21.33-
lip NEC
(acquired)
K13.0
congenital
Q38.0
liver
(congenital)
Q44.7
acquired
K76.89
lumbosacral
(congenital) (joint) (region)
Q76.49
acquired
M43.8
kyphosis
Kyphosis, congenital
lordosis
Lordosis, congenital
lung
(congenital)
Q33.9
acquired
J98.4
lymphatic system, congenital
Q89.9
Madelung's
(radius)
Q74.0
mandible
(acquired) (congenital)
M26.9
maxilla
(acquired) (congenital)
M26.9
meninges or membrane
(congenital)
Q07.9
cerebral
Q04.8
acquired
G96.19
spinal cord
(congenital)
G96.19
acquired
G96.19
metacarpus
(acquired)
Deformity, limb, forearm
congenital
Q74.0
metatarsus
(acquired)
Deformity, foot
congenital
Q66.9
middle ear
(congenital)
Q16.4
ossicles
Q16.3
mitral
(leaflets) (valve)
I05.8
parachute
Q23.2
stenosis, congenital
Q23.2
mouth
(acquired)
K13.79
congenital
Q38.6
multiple, congenital NEC
Q89.7
muscle
(acquired)
M62.89
congenital
Q79.9
sternocleidomastoid
Q68.0
musculoskeletal system
(acquired)
M95.9
congenital
Q79.9
specified NEC
M95.8
nail
(acquired)
L60.8
congenital
Q84.6
nasal
Deformity, nose
neck
(acquired)
M95.3
congenital
Q18.9
sternocleidomastoid
Q68.0
nervous system
(congenital)
Q07.9
nipple
(congenital)
Q83.9
acquired
N64.89
nose
(acquired) (cartilage)
M95.0
bone
(turbinate)
M95.0
congenital
Q30.9
bent or squashed
Q67.4
saddle
M95.0
syphilitic
A50.57
septum
(acquired)
J34.2
congenital
Q30.8
sinus
(wall) (congenital)
Q30.8
acquired
M95.0
syphilitic
(congenital)
A50.57
late
A52.73
ocular muscle
(congenital)
Q10.3
acquired
Strabismus, mechanical
opticociliary vessels
(congenital)
Q13.2
orbit
(eye) (acquired)
H05.30
atrophy
Atrophy, orbit
congenital
Q10.7
due to
bone disease NEC
H05.32-
trauma or surgery
H05.33-
enlargement
Enlargement, orbit
exostosis
Exostosis, orbit
organ of Corti
(congenital)
Q16.5
ovary
(congenital)
Q50.39
acquired
N83.8
oviduct, acquired
N83.8
palate
(congenital)
Q38.5
acquired
M27.8
cleft
(congenital)
Cleft, palate
pancreas
(congenital)
Q45.3
acquired
K86.89
parathyroid
(gland)
Q89.2
parotid
(gland) (congenital)
Q38.4
acquired
K11.8
patella
(acquired)
Disorder, patella, specified NEC
pelvis, pelvic
(acquired) (bony)
M95.5
with disproportion
(fetopelvic)
O33.0
causing obstructed labor
O65.0
congenital
Q74.2
rachitic sequelae
(late effect)
E64.3
penis
(glans) (congenital)
Q55.69
acquired
N48.89
pericardium
(congenital)
Q24.8
acquired
Pericarditis
pharynx
(congenital)
Q38.8
acquired
J39.2
pinna, acquired
Disorder, pinna, deformity
congenital
Q17.9
pituitary
(congenital)
Q89.2
posture
Dorsopathy, deforming
prepuce
(congenital)
Q55.69
acquired
N47.8
prostate
(congenital)
Q55.4
acquired
N42.89
pupil
(congenital)
Q13.2
acquired
Abnormality, pupillary
pylorus
(congenital)
Q40.3
acquired
K31.89
rachitic, old or healed
(acquired)
E64.3
radius
(acquired)
Deformity, limb, forearm
congenital
Q68.8
rectum
(congenital)
Q43.9
acquired
K62.89
reduction, congenital
(extremity) (limb)
Q73.8
condition and site
brain
Q04.3
lower
Defect, reduction, lower limb
upper
Defect, reduction, upper limb
renal
Deformity, kidney
respiratory system
(congenital)
Q34.9
rib
(acquired)
M95.4
congenital
Q76.6
cervical
Q76.5
rotation
(joint) (acquired)
Deformity, limb, specified site NEC
congenital
Q74.9
hip
Deformity, limb, specified type NEC, thigh
congenital
Q65.89
sacroiliac joint
(congenital)
Q74.2
acquired
M43.8
sacrum
(acquired)
M43.8
saddle
back
Lordosis
nose
M95.0
syphilitic
A50.57
salivary gland or duct
(congenital)
Q38.4
acquired
K11.8
scapula
(acquired)
M95.8
congenital
Q68.8
scrotum
(congenital)
Malformation, testis and scrotum
acquired
N50.89
seminal vesicles
(congenital)
Q55.4
acquired
N50.89
septum, nasal
(acquired)
J34.2
shoulder
(joint) (acquired)
Deformity, limb, upper arm
congenital
Q74.0
contraction
Contraction, joint, shoulder
sigmoid
(flexure) (congenital)
Q43.9
acquired
K63.89
skin
(congenital)
Q82.9
skull
(acquired)
M95.2
congenital
Q75.8
with
anencephaly
Q00.0
encephalocele
Encephalocele
hydrocephalus
Q03.9
with spina bifida
Spina bifida, by site, with hydrocephalus
microcephaly
Q02
soft parts, organs or tissues
(of pelvis)
in pregnancy or childbirth NEC
O34.8-
causing obstructed labor
O65.5
spermatic cord
(congenital)
Q55.4
acquired
N50.89
torsion
Torsion, spermatic cord
spinal
Dorsopathy, deforming
column
(acquired)
Dorsopathy, deforming
congenital
Q67.5
cord
(congenital)
Q06.9
acquired
G95.89
nerve root
(congenital)
Q07.9
spine
(acquired)
Dorsopathy, deforming
congenital
Q67.5
rachitic
E64.3
specified NEC
Dorsopathy, deforming, specified NEC
spleen
acquired
D73.89
congenital
Q89.09
Sprengel's
(congenital)
Q74.0
sternocleidomastoid, congenital
(muscle)
Q68.0
sternum
(acquired)
M95.4
congenital NEC
Q76.7
stomach
(congenital)
Q40.3
acquired
K31.89
submandibular gland
(congenital)
Q38.4
submaxillary gland
(congenital)
Q38.4
acquired
K11.8
talipes
Talipes
testis
(congenital)
Malformation, testis and scrotum
acquired
N44.8
torsion
Torsion, testis
thigh
(acquired)
Deformity, limb, thigh
congenital NEC
Q68.8
thorax
(acquired) (wall)
M95.4
congenital
Q67.8
sequelae of rickets
E64.3
thumb
(acquired)
Deformity, finger
congenital NEC
Q68.1
thymus
(tissue) (congenital)
Q89.2
thyroid
(gland) (congenital)
Q89.2
cartilage
Q31.8
acquired
J38.7
tibia
(acquired)
Deformity, limb, specified type NEC, lower leg
congenital NEC
Q68.8
saber
(syphilitic)
A50.56
toe
(acquired)
M20.6-
congenital
Q66.9
hallux rigidus
M20.2-
hallux valgus
M20.1-
hallux varus
M20.3-
hammer toe
M20.4-
specified NEC
M20.5X-
tongue
(congenital)
Q38.3
acquired
K14.8
tooth, teeth
K00.2
trachea
(rings) (congenital)
Q32.1
acquired
J39.8
transverse aortic arch
(congenital)
Q25.49
tricuspid
(leaflets) (valve)
I07.8
atresia or stenosis
Q22.4
Ebstein's
Q22.5
trunk
(acquired)
M95.8
congenital
Q89.9
ulna
(acquired)
Deformity, limb, forearm
congenital NEC
Q68.8
urachus, congenital
Q64.4
ureter
(opening) (congenital)
Q62.8
acquired
N28.89
urethra
(congenital)
Q64.79
acquired
N36.8
urinary tract
(congenital)
Q64.9
urachus
Q64.4
uterus
(congenital)
Q51.9
acquired
N85.8
uvula
(congenital)
Q38.5
vagina
(acquired)
N89.8
congenital
Q52.4
valgus NEC
M21.00
ankle
M21.07-
elbow
M21.02-
hip
M21.05-
knee
M21.06-
valve, valvular
(congenital) (heart)
Q24.8
acquired
Endocarditis
varus NEC
M21.10
ankle
M21.17-
elbow
M21.12-
hip
M21.15
knee
M21.16-
tibia
Osteochondrosis, juvenile, tibia
vas deferens
(congenital)
Q55.4
acquired
N50.89
vein
(congenital)
Q27.9
great
Q26.9
vertebra
Dorsopathy, deforming
vertical talus
(congenital)
Q66.80
left foot
Q66.82
right foot
Q66.81
vesicourethral orifice
(acquired)
N32.89
congenital NEC
Q64.79
vessels of optic papilla
(congenital)
Q14.2
visual field
(contraction)
Defect, visual field
vitreous body, acquired
H43.89
vulva
(congenital)
Q52.79
acquired
N90.89
wrist
(joint) (acquired)
Deformity, limb, forearm
congenital
Q68.8
contraction
Contraction, joint, wrist