| K |
| 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 |
| sarcoma |
| 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 |
| 46,X |
| iso(Xq) Q96.1 |
| 46,XX Q98.3 |
| with streak gonads Q50.32 |
| hermaphrodite(true) Q99.1 |
| male Q98.3 |
| 46,XY |
| 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 |
| cornea --see Opacity, cornea |
| 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 |
| with ulceration(central) (marginal) (perforated) (ring) --see Ulcer, cornea |
| actinic --see Photokeratitis |
| 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 |
| in(due to) |
| acanthamebiasis B60.13 |
| adenovirus B30.0 |
| exanthema --see also ExanthemB09 |
| 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 |
| parenchymatous --see Keratitis, interstitial |
| petrificans H16.8 |
| postmeasles B05.81 |
| punctata |
| leprosa A30.9H16.14- |
| syphilitic(profunda) A50.31 |
| 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- |
| with conjunctivitis --see Keratoconjunctivitis |
| due to light --see Photokeratitis |
| suppurative H16.8 |
| syphilitic(congenital) (prenatal) A50.31 |
| trachomatous A71.1 |
| sequelae B94.0 |
| tuberculous A18.52 |
| vesicular H16.8 |
| xerotic --see also KeratomalaciaH16.8 |
| 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 |
| in exanthema --see also ExanthemB09 |
| infectious B30.0 |
| lagophthalmic --see Keratoconjunctivitis, specified type NEC |
| 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 |
| in diseases classified elsewhere L86 |
| climactericum L85.1 |
| gonococcal A54.89 |
| gonorrheal A54.89 |
| punctata L85.2 |
| Reiter's --see Reiter's disease |
| 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 |
| nigricans L83 |
| obturans, external ear(canal) --see Cholesteatoma, external ear |
| 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 P55.0-P55.9) P57.0 |
| specified type NEC P57.8 |
| Keshan disease E59 |
| Ketoacidosis E87.2 |
| diabetic --see Diabetes, by type, with ketoacidosis |
| Ketonuria R82.4 |
| Ketosis NEC E88.89 |
| diabetic --see Diabetes, by type, with with ketoacidosis |
| Kew Garden fever A79.1 |
| Kidney --see condition |
| Kienböck's disease --see also Osteochondrosis, juvenile, hand, carpal lunate |
| adult M93.1 |
| Kimmelstiel(-Wilson) disease --see Diabetes, Kimmelstiel (-Wilson) disease |
| Kimura disease D21.9 |
| specified site(see Neoplasm, connective tissue benign) |
| Kink, kinking |
| artery I77.1 |
| hair(acquired) L67.8 |
| ileum or intestine --see Obstruction, intestine |
| Lane's --see Obstruction, intestine |
| organ or site, congenital NEC --see Anomaly, by site |
| ureter(pelvic junction) N13.5 |
| with |
| 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 GlomerulonephritisN05.- |
| 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(-Déjerine) 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 |
| infection --see Tuberculosis |
| relapsing fever A68.9 |
| Koch-Weeks' conjunctivitis --see Conjunctivitis, acute, mucopurulent |
| Köebner's syndrome Q81.8 |
| Köenig's disease(osteochondritis dissecans) --see Osteochondritis, dissecans |
| Köhler-Pellegrini-Steida disease or syndrome(calcification, knee joint) --see Bursitis, tibial collateral |
| Köhler's disease |
| patellar --see Osteochondrosis, juvenile, patella |
| tarsal navicular --see Osteochondrosis, juvenile, tarsus |
| 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 |
| drug-induced |
| due to drug abuse --see Abuse, drug, by type, with amnestic disorder |
| due to drug dependence --see Dependence, drug, by type, with amnestic disorder |
| nonalcoholic F04 |
| 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 |
| spindle --see Pigmentation, cornea, posterior |
| tumor C79.6- |
| Kufs' disease E75.4 |
| Kugelberg-Welander disease G12.1 |
| Kuhnt-Junius degeneration --see also Degeneration, maculaH35.32 |
| Kümmell's disease or spondylitis --see Spondylopathy, traumatic |
| Kupffer cell sarcoma C22.3 |
| Kuru A81.81 |
| Kussmaul's |
| disease M30.0 |
| respiration E87.2 |
| in diabetic acidosis --see Diabetes, by type, with ketoacidosis |
| Kwashiorkor E40 |
| marasmic, marasmus type E42 |
| Kyasanur Forest disease A98.2 |
| Kyphoscoliosis, kyphoscoliotic(acquired) --see also ScoliosisM41.9 |
| 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 M49.8E76.219 |
| 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 |