ICD 10 CM Index

Jaccoud''s syndrome see Arthropathy, postrheumatic, chronic
Jackson's
membrane   Q43.3
paralysis or syndrome   G83.89
veil   Q43.3
Jacquet''s dermatitis (diaper dermatitis) L22
Jadassohn-Pellizari''s disease or anetoderma   L90.2
Jadassohn's
Jaffe-Lichtenstein (-Uehlinger)syndrome see Dysplasia, fibrous, bone NEC
Jakob-Creutzfeldt disease or syndrome see Creutzfeldt-Jakob disease or syndrome
Jaksch-Luzet disease   D64.89
Jamaican
Janet''s disease   F48.8
Janiceps   Q89.4
Jansky-Bielschowsky amaurotic idiocy   E75.4
Japanese
B-type encephalitis   A83.0
river fever   A75.3
Jaundice (yellow) R17
acquired   D59.8
breast-milk (inhibitor)   P59.3
catarrhal (acute)    B15.9
with hepatic coma   B15.0
delayed conjugation   P59.8
associated with (due to)preterm delivery   P59.0
preterm delivery   P59.0
epidemic (catarrhal)    B15.9
with hepatic coma   B15.0
leptospiral   A27.0
spirochetal   A27.0
familial nonhemolytic (congenital) (Gilbert)    E80.4
Crigler-Najjar   E80.5
febrile (acute)    B15.9
with hepatic coma   B15.0
leptospiral   A27.0
spirochetal   A27.0
hematogenous   D59.9
hemolytic (acquired)    D59.9
hemorrhagic (acute) (leptospiral) (spirochetal)   A27.0
infectious (acute) (subacute)    B15.9
with hepatic coma   B15.0
leptospiral   A27.0
spirochetal   A27.0
leptospiral (hemorrhagic)   A27.0
malignant (without coma)    K72.90
with coma   K72.91
newborn    P59.9
antibodies   P55.1
incompatibility, maternalfetal   P55.1
isoimmunization   P55.1
absence or deficiency of enzyme system for bilirubin conjugation (congenital)   P59.8
bleeding   P58.1
breast milk inhibitors to conjugation    P59.3
associated with preterm delivery   P59.0
bruising   P58.0
Crigler-Najjar syndrome   E80.5
delayed conjugation    P59.8
associated with preterm delivery   P59.0
given to newborn   P58.42
transmitted from mother   P58.41
excessive hemolysis    P58.9
bleeding   P58.1
bruising   P58.0
given to newborn    P58.42
transmitted from mother    P58.41
infection   P58.2
polycythemia   P58.3
swallowed maternal blood   P58.5
specified type NEC   P58.8
galactosemia   E74.21
Gilbert syndrome   E80.4
hemolytic disease    P55.9
ABO isoimmunization   P55.1
Rh isoimmunization   P55.0
specified NEC   P55.8
hepatocellular damage    P59.20
specified NEC   P59.29
hereditary hemolytic anemia   P58.8
hypothyroidism, congenital   E03.1
incompatibility, maternalfetal NOS   P55.9
infection   P58.2
inspissated bile syndrome   P59.1
isoimmunization NOS   P55.9
mucoviscidosis   E84.9
polycythemia   P58.3
preterm delivery   P59.0
antibodies   P55.0
incompatibility, maternalfetal   P55.0
isoimmunization   P55.0
specified cause NEC   P59.8
swallowed maternal blood   P58.5
spherocytosis (congenital)   D58.0
nonhemolytic congenital familial (Gilbert)   E80.4
nuclear, newborn (see also Kernicterus of newborn)   P57.9
obstructive (see also Obstruction, bile duct)   K83.1
regurgitation (see also Obstruction, bile duct)   K83.1
spirochetal (hemorrhagic)   A27.0
newborn   P59.9
Jaw see condition
Jaw-winking phenomenon or syndrome   Q07.8
Jealousy
alcoholic   F10.988
childhood   F93.8
sibling   F93.8
Jejunitis see Enteritis
Jejunostomy status   Z93.4
Jejunum, jejunal see condition
Jensen''s disease see Inflammation, chorioretinal, focal, juxtapapillary
Jerks, myoclonic   G25.3
Jervell-Lange-Nielsen syndrome   I45.81
Jeune''s disease   Q77.2
Jigger disease   B88.1
Job''s syndrome (chronic granulomatous disease) D71
Joint see also condition
knee   M23.4-
Jordan''s anomaly or syndrome   D72.0
Joseph-Diamond-Blackfan anemia (congenital hypoplastic)   D61.01
Jungle yellow fever   A95.0
Jngling''s disease see Sarcoidosis
Juvenile see condition