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2009 ICD-9-CM
Diseases and Injuries
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Jaundice (yellow) 782.4 | |
acholuric (familial) (splenomegalic) (see also Spherocytosis) 282.0 | |
acquired 283.9 | |
breast milk 774.39 | |
catarrhal (acute) 070.1 | |
with hepatic coma 070.0 | |
chronic 571.9 | |
epidemic - see Jaundice, epidemic | |
cholestatic (benign) 782.4 | |
chronic idiopathic 277.4 | |
epidemic (catarrhal) 070.1 | |
with hepatic coma 070.0 | |
leptospiral 100.0 | |
spirochetal 100.0 | |
febrile (acute) 070.1 | |
with hepatic coma 070.0 | |
leptospiral 100.0 | |
spirochetal 100.0 | |
fetus or newborn 774.6 | |
due to or associated with | |
ABO | |
antibodies 773.1 | |
incompatibility, maternal/fetal 773.1 | |
isoimmunization 773.1 | |
absence or deficiency of enzyme system for bilirubin conjugation (congenital) 774.39 | |
blood group incompatibility NEC 773.2 | |
breast milk inhibitors to conjugation 774.39 | |
associated with preterm delivery 774.2 | |
bruising 774.1 | |
Crigler-Najjar syndrome 277.4 [774.31] | |
delayed conjugation 774.30 | |
associated with preterm delivery 774.2 | |
development 774.39 | |
drugs or toxins transmitted from mother 774.1 | |
G-6-PD deficiency 282.2 [774.0] | |
galactosemia 271.1 [774.5] | |
Gilbert's syndrome 277.4 [774.31] | |
hepatocellular damage 774.4 | |
hereditary hemolytic anemia (see also Anemia, hemolytic) 282.9 [774.0] | |
hypothyroidism, congenital 243 [774.31] | |
incompatibility, maternal/fetal NEC 773.2 | |
infection 774.1 | |
inspissated bile syndrome 774.4 | |
isoimmunization NEC 773.2 | |
mucoviscidosis 277.01 [774.5] | |
obliteration of bile duct, congenital 751.61 [774.5] | |
polycythemia 774.1 | |
preterm delivery 774.2 | |
red cell defect 282.9 [774.0] | |
Rh | |
antibodies 773.0 | |