J |
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 |
blue nevus --see Nevus |
intraepidermal epithelioma --see Neoplasm, skin, benign |
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 |
neuropathy G92 |
paraplegic tropical ataxic-spastic syndrome G92 |
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 |
acholuric(familial) (splenomegalic) --see also Spherocytosis |
acquired D59.8 |
breast-milk(inhibitor) P59.3 |
catarrhal(acute) B15.9 |
with hepatic coma B15.0 |
cholestatic(benign) R17 |
due to or associated with |
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 |
congenital --see Spherocytosis |
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 |
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(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 |
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(congenital) D58.0 |
neonatal --see Jaundice, newborn |
nonhemolytic congenital familial(Gilbert) E80.4 |
nuclear, newborn --see also Kernicterus of newbornP57.9 |
obstructive --see also Obstruction, bile ductK83.1 |
post-immunization --see Hepatitis, viral, type, B |
post-transfusion --see Hepatitis, viral, type, B |
regurgitation --see also Obstruction, bile ductK83.1 |
serum(homologous) (prophylactic) (therapeutic) --see Hepatitis, viral, type, B |
spirochetal(hemorrhagic) 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(chronic granulomatous disease) D71 |
Joint --see also condition |
mice --see Loose, body, joint |
knee M23.4- |
Jordan's anomaly or syndrome D72.0 |
Joseph-Diamond-Blackfan anemia(congenital hypoplastic) D61.01 |
Jungle yellow fever A95.0 |
Jüngling's disease --see Sarcoidosis |
Juvenile --see condition |