Inspissated bile syndrome
(newborn)
P59.1
Institutionalization, affecting child
Z62.22
disinhibited attachment
F94.2
Insufficiency, insufficient
accommodation, old age
H52.4
anatomic crown height
K08.89
anterior guidance
(occlusal)
M26.54
mitral disease
(valve)
I08.0
with tricuspid disease
(valve)
I08.3
tricuspid disease
(valve)
I08.2
with mitral disease
(valve)
I08.3
mitral disease
(valve)
I08.0
with tricuspid disease
(valve)
I08.3
with mitral disease
(valve)
I08.0
with tricuspid disease
(valve)
I08.3
tricuspid disease
(valve)
I08.2
with mitral disease
(valve)
I08.3
carotid
(hemispheric)
G45.1
coronary
(acute or subacute)
I24.8
precerebral
(multiple) (bilateral)
G45.2
cardiac
Insufficiency, myocardial
due to presence of prosthesis
(cardiac)
I97.11-
cardiorenal, hypertensive
I13.2
cardiovascular
Disease, cardiovascular
cerebrovascular
(acute)
I67.81
with transient focal neurological signs and symptoms
G45.8
clinical crown length
K08.89
coronary
(acute or subacute)
I24.8
chronic or with a stated duration of over 4 weeks
I25.89
heart
Insufficiency, myocardial
idiopathic autonomic
G90.09
interocclusal distance of fully erupted teeth
(ridge)
M26.36
lacrimal
(secretion)
H04.12-
passages
Stenosis, lacrimal
lung
Insufficiency, pulmonary
mental
(congenital)
Disability, intellectual
aortic valve disease
I08.0
with tricuspid disease
(valve)
I08.3
obstruction or stenosis
I05.2
with aortic valve disease
I08.0
tricuspid disease
(valve)
I08.1
with aortic disease
(valve)
I08.3
aortic valve disease
I08.0
with tricuspid disease
(valve)
I08.3
obstruction or stenosis
I05.2
with aortic valve disease
I08.0
with tricuspid disease
(valve)
I08.3
tricuspid disease
(valve)
I08.1
with aortic disease
(valve)
I08.3
with chorea, rheumatic
(Sydenham's)
I02.0
specified cause, except rheumatic
I34.0
heart
Insufficiency, myocardial
myocardial, myocardium
(with arteriosclerosis)
I50.9
Failure, heart
rheumatic fever
(conditions in I00)
I09.0
active, acute or subacute
I01.2
inactive or quiescent
(with chorea)
I09.0
hypertensive
Hypertension, heart
active, acute, or subacute
I01.2
peripheral vascular
(arterial)
I73.9
prenatal care affecting management of pregnancy
O09.3-
progressive pluriglandular
E31.0
acute, following surgery
(nonthoracic)
J95.2
chronic, following surgery
J95.3
with aortic, mitral or tricuspid disease
(valve)
I08.8
tarso-orbital fascia, congenital
Q10.3
thyroid
(gland) (acquired)
E03.9
tricuspid
(valve) (rheumatic)
I07.1
aortic disease
(valve)
I08.2
with mitral disease
(valve)
I08.3
mitral disease
(valve)
I08.1
with aortic disease
(valve)
I08.3
obstruction or stenosis
I07.2
with aortic disease
(valve)
I08.2
with mitral disease
(valve)
I08.3
valve, valvular
(heart)
I38
aortic
Insufficiency, aortic (valve)
mitral
Insufficiency, mitral (valve)
pulmonary
Insufficiency, pulmonary, valve
tricuspid
Insufficiency, tricuspid (valve)
acute
K55.059
Ischemia, intestine, acute
renal
Hypertension, kidney
venous
(chronic) (peripheral)
I87.2
ventricular
Insufficiency, myocardial
Intraabdominal testis, testes
Intrauterine contraceptive device
immediately following removal
Z30.433
retention in pregnancy
O26.3-
Intubation, difficult or failed
T88.4
Intussusception
(bowel) (colon) (enteric) (ileocecal) (ileocolic) (intestine) ( rectum)
K56.1
ureter
(with obstruction)
N13.5
Invagination
(bowel, colon, intestine or rectum)
K56.1
Involuntary movement, abnormal
R25.9
Iridoplegia
(complete) (partial) (reflex)
H57.09
Irradiation effects, adverse
T66
Irreducible, irreducibility
condition
Iselin's disease or osteochondrosis
Osteochondrosis, juvenile, metatarsus
Islet cell tumor, pancreas
D13.7
Isomerism atrial appendages
(with asplenia or polysplenia)
Q20.6
Isosporiasis, isosporosis
A07.3
Ivemark's syndrome
(asplenia with congenital heart disease)
Q89.01
Jaccoud's syndrome
Arthropathy, postrheumatic, chronic
Jadassohn-Pellizari's disease or anetoderma
L90.2
Jaffe-Lichtenstein syndrome
(-Uehlinger)
Dysplasia, fibrous, bone NEC
Jakob-Creutzfeldt disease or syndrome
Creutzfeldt-Jakob disease or syndrome
Jansky-Bielschowsky amaurotic idiocy
E75.4
Jaw-winking phenomenon or syndrome
Q07.8
Jensen's disease
Inflammation, chorioretinal, focal, juxtapapillary
Jervell-Lange-Nielsen syndrome
I45.81
Job's syndrome
(chronic granulomatous disease)
D71
Jordan's anomaly or syndrome
D72.0
Joseph-Diamond-Blackfan anemia
(congenital hypoplastic)
D61.01
Kartagener's syndrome or triad
(sinusitis, bronchiectasis, situs inversus)
Q89.3
Katayama's disease or fever
B65.2
Kayser-Fleischer ring
(cornea) (pseudosclerosis)
H18.04-
Kaznelson's syndrome
(congenital hypoplastic anemia)
D61.01
Kelly
(-Patterson) syndrome (sideropenic dysphagia)
D50.1
Keratinization of alveolar ridge mucosa
Keratinized residual ridge mucosa
Keratitis
(nodular) (nonulcerative) (simple) (zonular)
H16.9
with ulceration
(central) (marginal) (perforated) (ring)
Ulcer, cornea
arborescens
(herpes simplex)
B00.52
specified type NEC
H16.399
dendritic
(a) (herpes simplex)
B00.52
disciform
(is) (herpes simplex)
B00.52
gonococcal
(congenital or prenatal)
A54.33
herpes, herpetic
(simplex)
B00.52
herpes virus
(simplex)
B00.52
interstitial
(nonsyphilitic)
H16.30-
herpes, herpetic
(simplex)
B00.52
specified type NEC
H16.39-
syphilitic
(congenital) (late)
A50.31
parenchymatous
Keratitis, interstitial
syphilitic
(profunda)
A50.31
with conjunctivitis
Keratoconjunctivitis
due to light
Photokeratitis
syphilitic
(congenital) (prenatal)
A50.31
xerotic
H16.8
Keratomalacia
vitamin A deficiency
E50.4
Keratocyst
(dental) (odontogenic)
Cyst, calcifying odontogenic
Keratoderma, keratodermia
(congenital) (palmaris et plantaris) (symmetrical)
Q82.8
in diseases classified elsewhere
L86
Keratohemia
Pigmentation, cornea, stromal
Keratoscleritis, tuberculous
A18.52
Kernicterus of newborn
(not due to isoimmunization)
P57.9
due to isoimmunization
(conditions in P55.0-P55.9)
P57.0
Kienböck's disease
Osteochondrosis, juvenile, hand, carpal lunate
Kimmelstiel disease
(-Wilson)
Diabetes, Kimmelstiel (-Wilson) disease
Kinnier Wilson's disease
(hepatolenticular degeneration)
E83.01
Klebsiella pneumoniae, as cause of disease classified elsewhere
(K.)
B96.1
Klippel-Feil deficiency, disease, or syndrome
(brevicollis)
Q76.1
Klippel-Trenaunay syndrome
(-Weber)
Q87.2
Klumpke
(-Déjerine) palsy, paralysis (birth) (newborn)
P14.1
Koch-Weeks' conjunctivitis
Conjunctivitis, acute, mucopurulent
Köenig's disease
(osteochondritis dissecans)
Osteochondritis, dissecans
Köhler-Pellegrini-Steida disease or syndrome
(calcification, knee joint)
Bursitis, tibial collateral
Korsakoff's
(Wernicke) disease, psychosis or syndrome (alcoholic)
F10.96
due to drug abuse
Abuse, drug, by type, with amnestic disorder
due to drug dependence
Dependence, drug, by type, with amnestic disorder
Korsakov's disease, psychosis or syndrome
Korsakoff's disease
Korsakow's disease, psychosis or syndrome
Korsakoff's disease
Kostmann's disease or syndrome
(infantile genetic agranulocytosis)
Agranulocytosis
Kraft-Weber-Dimitri disease
Q85.8
Kugelberg-Welander disease
G12.1
Kuhnt-Junius degeneration
H35.32-
Degeneration, macula
Kümmell's disease or spondylitis
Spondylopathy, traumatic
Kyphoscoliosis, kyphoscoliotic
(acquired)
M41.9
Scoliosis