- Kahler disease
C90.0
- Kakke
E51.1
- Kala-azar
B55.0
- Kallmann's syndrome
E23.0
- Kanner's syndrome
F84.0
- Kaposi's
- sarcoma
- connective tissue
C46.1
- lymph node (multiple)
C46.3
- multiple organs
C46.8
- palate (hard) (soft)
C46.2
- resulting from HIV disease
B21.0
- skin (multiple sites)
C46.0
- specified site NEC
C46.7
- unspecified site
C46.9
- varicelliform eruption
B00.0
- Kartagener's syndrome or triad
Q89.3
- Karyotype - see also
condition
- Kaschin-Beck disease
M12.1
- Katayama's disease or fever
B65.2
- Kawasaki's syndrome
M30.3
- Kayser-Fleischer ring (cornea)
H18.0
- Kearns-Sayre syndrome
H49.8
- Kelis
L91.0
- Kelly-Paterson syndrome
D50.1
- Keloid, cheloid
L91.0
- Keratectasia
H18.7
- Keratitis (nonulcerative)
H16.9
- Keratoacanthoma
L85.8
- Keratocele
H18.7
- Keratoconjunctivitis
H16.2
- Keratoconus
H18.6
- Keratocyst (odontogenic) (of)
D16.5
- Keratoderma, keratodermia (congenital) (palmaris et plantaris) (symmetrical)
Q82.8
- Keratodermatocele
H18.7
- Keratoglobus
H18.7
- Keratohemia
H18.0
- Keratoiritis Iridocyclitis
H20.9
- Keratoma
L57.0
- palmaris et plantaris hereditarium
Q82.8
- senile
L57.0
- Keratomalacia
H18.4
- Keratomegaly
Q13.4
- Keratomycosis
B49†
H19.2*
- nigrans, nigricans (palmaris)
B36.1
- Keratopathy
H18.9
- Keratoscleritis, tuberculous
A18.5†
H19.2*
- Keratosis
L57.0
- Kerato-uveitis Iridocyclitis
H20.9
- Kerion (celsi)
B35.0
- Kernicterus of newborn
P57.9
- due to isoimmunization (conditions in P55.-)
P57.0
- specified type NEC
P57.8
- Keshan disease
E59
- Ketoacidosis NEC
E87.2
- Ketonuria
R82.4
- Ketosis NEC
E88.8
- Kew Garden fever
A79.1
- Kidney - see
condition
- Kienböck's disease or osteochondrosis
M92.2
- Kimmelstiel(-Wilson) disease or syndrome (diabetic glomerulosclerosis)
- code
to E10-E14 with fourth character .2
- Kimura disease
D21.9
- Kink
- Kinking hair (acquired)
L67.8
- Kissing spine
M48.2
- Klatskin's tumor
C24.0
- Klauder's disease
A26.8
- Klebs' disease Glomerulonephritis
N05.-
- Klebsiella (K.) pneumoniae, as cause of disease classified elsewhere
B96.1
- Kleine-Levin syndrome
G47.8
- Kleptomania
F63.2
- Klinefelter's syndrome
Q98.4
- karyotype 47,XXY
Q98.0
- male with
- karyotype 46,XX
Q98.2
- more than two X chromosomes
Q98.1
- Klippel-Feil deficiency or syndrome
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)
M21.0
- Knot (true), umbilical cord
O69.2
- affecting fetus or newborn
P02.5
- Knotting of hair
L67.8
- Knuckle pad (Garrod's)
M72.1
- Koch's infection Tuberculosis
A16.9
- Koch-Weeks' conjunctivitis
H10.0
- Koebner's syndrome
Q81.8
- Köhler's disease
- Koilonychia
L60.3
- Kojevnikov's, Kozhevnikof's epilepsy
G40.5
- Koplik's spots
B05.9
- Korsakov's disease, psychosis or syndrome (alcoholic)
F10.6
- Kostmann's disease
D70
- Krabbe's disease
E75.2
- Kraepelin-Morel disease Schizophrenia
F20.9
- Kraft-Weber-Dimitri disease
Q85.8
- Kraurosis
- Krukenberg's
- Kufs' disease
E75.4
- Kugelberg-Welander disease
G12.1
- Kuhnt-Junius degeneration
H35.3
- Kümmell's disease or spondylitis
M48.3
- Kupffer cell sarcoma
C22.3
- Kuru
A81.8
- Kussmaul's
- Kwashiorkor
E40
- marasmic, marasmus type
E42
- Kyasanur Forest disease
A98.2
- Kyphoscoliosis, kyphoscoliotic (acquired) Scoliosis
M41.9
- Kyphosis, kyphotic (acquired)
M40.2
- Kyrle's disease
L87.0