|
Kahler''s disease C90.0- |
|
|
Kakke E51.11 |
|
|
Kala-azar B55.0 |
|
|
Kallmann''s syndrome E23.0 |
|
|
Kanner''s syndrome (autism) see Psychosis, childhood |
|
|
Kaposi's |
|
|
dermatosis (xeroderma pigmentosum) Q82.1 |
|
|
lichen ruber L44.0 |
|
|
acuminatus L44.0 |
|
|
colon C46.4 |
|
|
connective tissue C46.1 |
|
|
gastrointestinal organ C46.4 |
|
|
lung C46.5- |
|
|
lymph node (multiple) C46.3 |
|
|
palate (hard) (soft) C46.2 |
|
|
rectum C46.4 |
|
|
skin (multiple sites) C46.0 |
|
|
specified site NEC C46.7 |
|
|
stomach C46.4 |
|
|
unspecified site C46.9 |
|
|
varicelliform eruption B00.0 |
|
|
vaccinia T88.1 |
|
|
Kartagener''s syndrome or triad (sinusitis, bronchiectasis, situs inversus) Q89.3 |
|
|
Karyotype |
|
|
with abnormality except iso (Xq) Q96.2 |
|
|
45,X Q96.0 |
|
|
iso (Xq) Q96.1 |
|
|
46,XX Q98.3 |
|
|
with streak gonads Q50.32 |
|
|
hermaphrodite (true) Q99.1 |
|
|
male Q98.3 |
|
|
with streak gonads Q56.1 |
|
|
female Q97.3 |
|
|
hermaphrodite (true) Q99.1 |
|
|
47,XXX Q97.0 |
|
|
47,XXY Q98.0 |
|
|
47,XYY Q98.5 |
|
|
Kaschin-Beck disease see Disease, Kaschin-Beck |
|
|
Katayama''s disease or fever B65.2 |
|
|
Kawasaki''s syndrome M30.3 |
|
|
Kayser-Fleischer ring (cornea) (pseudosclerosis) H18.04- |
|
|
Kaznelson''s syndrome (congenital hypoplastic anemia) D61.01 |
|
|
Kearns-Sayre syndrome H49.81- |
|
|
Kedani fever A75.3 |
|
|
Kelis L91.0 |
|
|
Kelly (-Patterson) syndrome (sideropenic dysphagia) D50.1 |
|
|
Keloid, cheloid L91.0 |
|
|
acne L73.0 |
|
|
Addison''s L94.0 |
|
|
Hawkin''s L91.0 |
|
|
scar L91.0 |
|
|
Keloma L91.0 |
|
|
Kenya fever A77.1 |
|
|
Keratectasia see also Ectasia, cornea |
|
|
congenital Q13.4 |
|
|
Keratinization of alveolar ridge mucosa |
|
|
excessive K13.23 |
|
|
minimal K13.22 |
|
|
Keratinized residual ridge mucosa |
|
|
excessive K13.23 |
|
|
minimal K13.22 |
|
|
Keratitis (nodular) (nonulcerative) (simple) (zonular) H16.9 |
|
|
arborescens (herpes simplex) B00.52 |
|
|
areolar H16.11- |
|
|
bullosa H16.8 |
|
|
deep H16.309 |
|
|
specified type NEC H16.399 |
|
|
dendritic (a) (herpes simplex) B00.52 |
|
|
disciform (is) (herpes simplex) B00.52 |
|
|
varicella B01.81 |
|
|
filamentary H16.12- |
|
|
gonococcal (congenital or prenatal) A54.33 |
|
|
herpes, herpetic (simplex) B00.52 |
|
|
zoster B02.33 |
|
|
acanthamebiasis B60.13 |
|
|
adenovirus B30.0 |
|
|
herpes (simplex)virus B00.52 |
|
|
measles B05.81 |
|
|
syphilis A50.31 |
|
|
tuberculosis A18.52 |
|
|
zoster B02.33 |
|
|
interstitial (nonsyphilitic) H16.30- |
|
|
diffuse H16.32- |
|
|
herpes, herpetic (simplex) B00.52 |
|
|
zoster B02.33 |
|
|
sclerosing H16.33- |
|
|
specified type NEC H16.39- |
|
|
syphilitic (congenital) (late) A50.31 |
|
|
tuberculous A18.52 |
|
|
macular H16.11- |
|
|
nummular H16.11- |
|
|
oyster shuckers'' H16.8 |
|
|
petrificans H16.8 |
|
|
postmeasles B05.81 |
|
|
syphilitic (profunda) A50.31 |
|
|
leprosa A309 H16.14- |
|
|
punctate H16.14- |
|
|
purulent H16.8 |
|
|
rosacea L71.8 |
|
|
sclerosing H16.33- |
|
|
specified type NEC H16.8 |
|
|
stellate H16.11- |
|
|
striate H16.11- |
|
|
superficial H16.10- |
|
|
suppurative H16.8 |
|
|
syphilitic (congenital) (prenatal) A50.31 |
|
|
trachomatous A71.1 |
|
|
sequelae B94.0 |
|
|
tuberculous A18.52 |
|
|
vesicular H16.8 |
|
|
xerotic (see also Keratomalacia) H16.8 |
|
|
vitamin A deficiency E50.4 |
|
|
Keratoacanthoma L85.8 |
|
|
Keratocele see Descemetocele |
|
|
Keratoconjunctivitis H16.20- |
|
|
Acanthamoeba B60.13 |
|
|
adenoviral B30.0 |
|
|
epidemic B30.0 |
|
|
exposure H16.21- |
|
|
herpes, herpetic (simplex) B00.52 |
|
|
zoster B02.33 |
|
|
infectious B30.0 |
|
|
neurotrophic H16.23- |
|
|
phlyctenular H16.25- |
|
|
postmeasles B05.81 |
|
|
shipyard B30.0 |
|
|
sicca (Sjogren''s) M35.0- |
|
|
not Sjogren''s H16.22- |
|
|
specified type NEC H16.29- |
|
|
tuberculous (phlyctenular) A18.52 |
|
|
vernal H16.26- |
|
|
Keratoconus H18.60- |
|
|
congenital Q13.4 |
|
|
stable H18.61- |
|
|
unstable H18.62- |
|
|
Keratocyst (dental) (odontogenic) see Cyst, calcifying odontogenic |
|
|
Keratoderma, keratodermia (congenital) (palmaris et plantaris) (symmetrical) Q82.8 |
|
|
acquired L85.1 |
|
|
climactericum L85.1 |
|
|
gonococcal A54.89 |
|
|
gonorrheal A54.89 |
|
|
punctata L85.2 |
|
|
Keratodermatocele see Descemetocele |
|
|
Keratoglobus H18.79 |
|
|
congenital Q15.8 |
|
|
with glaucoma Q15.0 |
|
|
Keratohemia see Pigmentation, cornea, stromal |
|
|
Keratoiritis see also Iridocyclitis |
|
|
syphilitic A50.39 |
|
|
tuberculous A18.54 |
|
|
Keratoma L57.0 |
|
|
palmaris and plantaris hereditarium Q82.8 |
|
|
senile L57.0 |
|
|
Keratomalacia H18.44- |
|
|
vitamin A deficiency E50.4 |
|
|
Keratomegaly Q13.4 |
|
|
Keratomycosis B49 |
|
|
nigrans, nigricans (palmaris) B36.1 |
|
|
Keratopathy H18.9 |
|
|
band H18.42- |
|
|
bullous H18.1- |
|
|
bullous (aphakic), following cataract surgery H59.01- |
|
|
Keratoscleritis, tuberculous A18.52 |
|
|
Keratosis L57.0 |
|
|
actinic L57.0 |
|
|
arsenical L85.8 |
|
|
congenital, specified NEC Q80.8 |
|
|
female genital NEC N94.89 |
|
|
follicularis Q82.8 |
|
|
acquired L11.0 |
|
|
congenita Q82.8 |
|
|
et parafollicularis in cutem penetrans L87.0 |
|
|
spinulosa (decalvans) Q82.8 |
|
|
vitamin A deficiency E50.8 |
|
|
gonococcal A54.89 |
|
|
male genital (external) N50.8 |
|
|
palmaris et plantaris (inherited) (symmetrical) Q82.8 |
|
|
acquired L85.1 |
|
|
penile N48.89 |
|
|
pharynx J39.2 |
|
|
pilaris, acquired L85.8 |
|
|
punctata (palmaris et plantaris) L85.2 |
|
|
scrotal N50.8 |
|
|
seborrheic L82.1 |
|
|
inflamed L82.0 |
|
|
senile L57.0 |
|
|
solar L57.0 |
|
|
tonsillaris J35.8 |
|
|
vagina N89.4 |
|
|
vegetans Q82.8 |
|
|
vitamin A deficiency E50.8 |
|
|
vocal cord J38.3 |
|
|
Kerato-uveitis see Iridocyclitis |
|
|
Kerunoparalysis T75.09 |
|
|
Kerion (celsi) B35.0 |
|
|
Kernicterus of newborn (not due to isoimmunization) P57.9 |
|
|
due to isoimmunization (conditions in P550-P559) P57.0 |
|
|
specified type NEC P57.8 |
|
|
Keshan disease E59 |
|
|
Ketoacidosis E87.2 |
|
|
Ketonuria R82.4 |
|
|
Ketosis NEC E88.89 |
|
|
Kew Garden fever A79.1 |
|
|
Kidney see condition |
|
|
Kienbck''s disease see also Osteochondrosis, juvenile, hand, carpal lunate |
|
|
adult M93.1 |
|
|
Kimmelstiel (-Wilson)disease see Diabetes, Kimmelstiel (-Wilson) disease |
|
|
Kimura disease D21.9 |
|
|
Kink, kinking |
|
|
artery I77.1 |
|
|
hair (acquired) L67.8 |
|
|
ureter (pelvic junction) N13.5 |
|
|
hydronephrosis N13.1 |
|
|
with infection N13.6 |
|
|
pyelonephritis (chronic) N11.1 |
|
|
congenital Q62.39 |
|
|
vein (s) I87.8 |
|
|
caval I87.1 |
|
|
peripheral I87.1 |
|
|
Kinnier Wilson''s disease (hepatolenticular degeneration) E83.01 |
|
|
Kissing spine M48.20 |
|
|
cervical region M48.22 |
|
|
cervicothoracic region M48.23 |
|
|
lumbar region M48.26 |
|
|
lumbosacral region M48.27 |
|
|
occipito-atlanto-axial region M48.21 |
|
|
thoracic region M48.24 |
|
|
thoracolumbar region M48.25 |
|
|
Klatskin''s tumor C24.0 |
|
|
Klauder''s disease A26.8 |
|
|
Klebs'' disease (see also Glomerulonephritis) N05.- |
|
|
Klebsiella (K)pneumoniae, as cause of disease classified elsewhere B96.1 |
|
|
Klein (e)-Levin syndrome G47.13 |
|
|
Kleptomania F63.2 |
|
|
Klinefelter''s syndrome Q98.4 |
|
|
karyotype 47,XXY Q98.0 |
|
|
male with more than two X chromosomes Q98.1 |
|
|
Klippel-Feil deficiency, disease, or syndrome (brevicollis) Q76.1 |
|
|
Klippel''s disease I67.2 |
|
|
Klippel-Trenaunay (-Weber)syndrome Q87.2 |
|
|
Klumpke (-Djerine) palsy, paralysis (birth) (newborn) P14.1 |
|
|
Knee see condition |
|
|
Knock knee (acquired) M21.06- |
|
|
congenital Q74.1 |
|
|
Knot (s) |
|
|
intestinal, syndrome (volvulus) K56.2 |
|
|
surfer S89.8- |
|
|
umbilical cord (true) O69.2 |
|
|
Knotting (of) |
|
|
hair L67.8 |
|
|
intestine K56.2 |
|
|
Knuckle pad (Garrod''s) M72.1 |
|
|
Koch's |
|
|
relapsing fever A68.9 |
|
|
Koch-Weeks'' conjunctivitis see Conjunctivitis, acute, mucopurulent |
|
|
Kebner''s syndrome Q81.8 |
|
|
Kenig''s disease (osteochondritis dissecans) see Osteochondritis, dissecans |
|
|
Khler-Pellegrini-Steida disease or syndrome (calcification, knee joint) see Bursitis, tibial collateral |
|
|
Khler''s disease |
|
|
Koilonychia L60.3 |
|
|
congenital Q84.6 |
|
|
Kojevnikov''s, epilepsy see Kozhevnikof''s epilepsy |
|
|
Koplik''s spots B05.9 |
|
|
Kopp''s asthma E32.8 |
|
|
Korsakoff''s (Wernicke) disease, psychosis or syndrome (alcoholic) F10.96 |
|
|
with dependence F10.26 |
|
|
Korsakov''s disease, psychosis or syndrome see Korsakoff''s disease |
|
|
Korsakow''s disease, psychosis or syndrome see Korsakoff''s disease |
|
|
Kostmann''s disease or syndrome (infantile genetic agranulocytosis) see Agranulocytosis |
|
|
Kozhevnikof''s epilepsy G40.109 |
|
|
intractable G40.119 |
|
|
with status epilepticus G40.111 |
|
|
without status epilepticus G40.119 |
|
|
not intractable G40.109 |
|
|
with status epilepticus G40.101 |
|
|
without status epilepticus G40.109 |
|
|
Krabbe's |
|
|
disease E75.23 |
|
|
syndrome, congenital muscle hypoplasia Q79.8 |
|
|
Kraepelin-Morel disease see Schizophrenia |
|
|
Kraft-Weber-Dimitri disease Q85.8 |
|
|
Kraurosis |
|
|
ani K62.89 |
|
|
penis N48.0 |
|
|
vagina N89.8 |
|
|
vulva N90.4 |
|
|
Kreotoxism A05.9 |
|
|
Krukenberg's |
|
|
tumor C79.6- |
|
|
Kufs'' disease E75.4 |
|
|
Kugelberg-Welander disease G12.1 |
|
|
Kuhnt-Junius degeneration (see also Degeneration, macula) H35.32 |
|
|
Kmmell''s disease or spondylitis see Spondylopathy, traumatic |
|
|
Kupffer cell sarcoma C22.3 |
|
|
Kuru A81.81 |
|
|
Kussmaul's |
|
|
disease M30.0 |
|
|
respiration E87.2 |
|
|
Kwashiorkor E40 |
|
|
Kyasanur Forest disease A98.2 |
|
|
Kyphoscoliosis, kyphoscoliotic (acquired) (see also Scoliosis) M41.9 |
|
|
congenital Q67.5 |
|
|
heart (disease) I27.1 |
|
|
sequelae of rickets E64.3 |
|
|
tuberculous A18.01 |
|
|
Kyphosis, kyphotic (acquired) M40.209 |
|
|
cervical region M40.202 |
|
|
cervicothoracic region M40.203 |
|
|
congenital Q76.419 |
|
|
cervical region Q76.412 |
|
|
cervicothoracic region Q76.413 |
|
|
occipito-atlanto-axial region Q76.411 |
|
|
thoracic region Q76.414 |
|
|
thoracolumbar region Q76.415 |
|
|
Morquio-Brailsford type (spinal) (see also subcategory M498) E76.219 |
|
|
postlaminectomy M96.3 |
|
|
postradiation therapy M96.2 |
|
|
postural (adolescent) M40.00 |
|
|
cervicothoracic region M40.03 |
|
|
thoracic region M40.04 |
|
|
thoracolumbar region M40.05 |
|
|
secondary NEC M40.10 |
|
|
cervical region M40.12 |
|
|
cervicothoracic region M40.13 |
|
|
thoracic region M40.14 |
|
|
thoracolumbar region M40.15 |
|
|
sequelae of rickets E64.3 |
|
|
specified type NEC M40.299 |
|
|
cervical region M40.292 |
|
|
cervicothoracic region M40.293 |
|
|
thoracic region M40.294 |
|
|
thoracolumbar region M40.295 |
|
|
syphilitic, congenital A50.56 |
|
|
thoracic region M40.204 |
|
|
thoracolumbar region M40.205 |
|
|
tuberculous A18.01 |
|
|
Kyrle disease L87.0 |
|
