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ICD-10-CM Index - Letter J
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Terms starting with 'J'
Jaccoud's syndrome
(see: Arthropathy, postrheumatic, chronic)
Jackson's
membrane
Q43.3
paralysis or syndrome
G83.89
veil
Q43.3
Jacquet's dermatitis
L22
Jadassohn-Pellizari's disease or anetoderma
L90.2
Jadassohn's
blue nevus (see: Nevus)
intraepidermal epithelioma (see: Neoplasm, skin, benign)
Jaffe-Lichtenstein
(see: Dysplasia, fibrous, bone NEC)
Jakob-Creutzfeldt disease or syndrome
(see: Creutzfeldt-Jakob disease or syndrome)
Jaksch-Luzet disease
D64.89
Jamaican
neuropathy
G92.8
paraplegic tropical ataxic-spastic syndrome
G92.8
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
R17
acholuric
acquired
D59.8
breast-milk
P59.3
catarrhal
B15.9
with hepatic coma
B15.0
cholestatic
R17
due to or associated with
delayed conjugation
P59.8
associated with
P59.0
preterm delivery
P59.0
epidemic
B15.9
with hepatic coma
B15.0
leptospiral
A27.0
spirochetal
A27.0
familial nonhemolytic
E80.4
Crigler-Najjar
E80.5
febrile
B15.9
with hepatic coma
B15.0
leptospiral
A27.0
spirochetal
A27.0
hematogenous
D59.9
hemolytic
D59.9
congenital (see: Spherocytosis)
hemorrhagic
A27.0
infectious
B15.9
with hepatic coma
B15.0
leptospiral
A27.0
spirochetal
A27.0
leptospiral
A27.0
malignant
K72.90
with coma
K72.91
newborn
P59.9
due to or associated with
ABO
antibodies
P55.1
incompatibility, maternal/fetal
P55.1
isoimmunization
P55.1
absence or deficiency of enzyme system for bilirubin conjugation
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
drugs or toxins
given to newborn
P58.42
transmitted from mother
P58.41
excessive hemolysis
P58.9
due to
bleeding
P58.1
bruising
P58.0
drugs or toxins
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, maternal/fetal 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
Rh
antibodies
P55.0
incompatibility, maternal/fetal
P55.0
isoimmunization
P55.0
specified cause NEC
P59.8
swallowed maternal blood
P58.5
spherocytosis
D58.0
neonatal (see: Jaundice, newborn)
nonhemolytic congenital familial
E80.4
nuclear, newborn
P57.9
obstructive
K83.1
post-immunization (see: Hepatitis, viral, type, B)
post-transfusion (see: Hepatitis, viral, type, B)
regurgitation
K83.1
serum (see: Hepatitis, viral, type, B)
spirochetal
A27.0
symptomatic
R17
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
D71
Joint
mice (see: Loose, body, joint)
knee
M23.4-
Jordan's anomaly or syndrome
D72.0
Joseph-Diamond-Blackfan anemia
D61.01
Jungle yellow fever
A95.0
Jüngling's disease
(see: Sarcoidosis)
Juvenile
(see: condition)