Jaundice (yellow)
- R17
- acholuric (familial) (splenomegalic)See see also Spherocytosis
- acholuric (familial) (splenomegalic), acquiredD59.8
- breast-milk (inhibitor)P59.3
- catarrhal (acute)B15.9
- catarrhal (acute), with hepatic comaB15.0
- cholestatic (benign)R17
- due to or associated with
- due to or associated with, delayed conjugationP59.8
- due to or associated with, delayed conjugation, associated with (due to) preterm deliveryP59.0
- due to or associated with, preterm deliveryP59.0
- epidemic (catarrhal)B15.9
- epidemic (catarrhal), with hepatic comaB15.0
- epidemic (catarrhal), leptospiralA27.0
- epidemic (catarrhal), spirochetalA27.0
- familial nonhemolytic (congenital) (Gilbert)E80.4
- familial nonhemolytic (congenital) (Gilbert), Crigler-NajjarE80.5
- febrile (acute)B15.9
- febrile (acute), with hepatic comaB15.0
- febrile (acute), leptospiralA27.0
- febrile (acute), spirochetalA27.0
- hematogenousD59.9
- hemolytic (acquired)D59.9
- hemolytic (acquired), congenitalSee Spherocytosis
- hemorrhagic (acute) (leptospiral) (spirochetal)A27.0
- infectious (acute) (subacute)B15.9
- infectious (acute) (subacute), with hepatic comaB15.0
- infectious (acute) (subacute), leptospiralA27.0
- infectious (acute) (subacute), spirochetalA27.0
- leptospiral (hemorrhagic)A27.0
- malignant (without coma)K72.90
- malignant (without coma), with comaK72.91
- newbornP59.9
- newborn, due to or associated with
- newborn, due to or associated with, ABO
- newborn, due to or associated with, ABO, antibodiesP55.1
- newborn, due to or associated with, ABO, incompatibility, maternal/fetalP55.1
- newborn, due to or associated with, ABO, isoimmunizationP55.1
- newborn, due to or associated with, absence or deficiency of enzyme system for bilirubin conjugation (congenital)P59.8
- newborn, due to or associated with, bleedingP58.1
- newborn, due to or associated with, breast milk inhibitors to conjugationP59.3
- newborn, due to or associated with, breast milk inhibitors to conjugation, associated with preterm deliveryP59.0
- newborn, due to or associated with, bruisingP58.0
- newborn, due to or associated with, Crigler-Najjar syndromeE80.5
- newborn, due to or associated with, delayed conjugationP59.8
- newborn, due to or associated with, delayed conjugation, associated with preterm deliveryP59.0
- newborn, due to or associated with, drugs or toxins
- newborn, due to or associated with, drugs or toxins, given to newbornP58.42
- newborn, due to or associated with, drugs or toxins, transmitted from motherP58.41
- newborn, due to or associated with, excessive hemolysisP58.9
- newborn, due to or associated with, excessive hemolysis, due to
- newborn, due to or associated with, excessive hemolysis, due to, bleedingP58.1
- newborn, due to or associated with, excessive hemolysis, due to, bruisingP58.0
- newborn, due to or associated with, excessive hemolysis, due to, drugs or toxins
- newborn, due to or associated with, excessive hemolysis, due to, drugs or toxins, given to newbornP58.42
- newborn, due to or associated with, excessive hemolysis, due to, drugs or toxins, transmitted from motherP58.41
- newborn, due to or associated with, excessive hemolysis, due to, infectionP58.2
- newborn, due to or associated with, excessive hemolysis, due to, polycythemiaP58.3
- newborn, due to or associated with, excessive hemolysis, due to, swallowed maternal bloodP58.5
- newborn, due to or associated with, excessive hemolysis, specified type NECP58.8
- newborn, due to or associated with, galactosemiaE74.21
- newborn, due to or associated with, Gilbert syndromeE80.4
- newborn, due to or associated with, hemolytic diseaseP55.9
- newborn, due to or associated with, hemolytic disease, ABO isoimmunizationP55.1
- newborn, due to or associated with, hemolytic disease, Rh isoimmunizationP55.0
- newborn, due to or associated with, hemolytic disease, specified NECP55.8
- newborn, due to or associated with, hepatocellular damageP59.20
- newborn, due to or associated with, hepatocellular damage, specified NECP59.29
- newborn, due to or associated with, hereditary hemolytic anemiaP58.8
- newborn, due to or associated with, hypothyroidism, congenitalE03.1
- newborn, due to or associated with, incompatibility, maternal/fetal NOSP55.9
- newborn, due to or associated with, infectionP58.2
- newborn, due to or associated with, inspissated bile syndromeP59.1
- newborn, due to or associated with, isoimmunization NOSP55.9
- newborn, due to or associated with, mucoviscidosisE84.9
- newborn, due to or associated with, polycythemiaP58.3
- newborn, due to or associated with, preterm deliveryP59.0
- newborn, due to or associated with, Rh
- newborn, due to or associated with, Rh, antibodiesP55.0
- newborn, due to or associated with, Rh, incompatibility, maternal/fetalP55.0
- newborn, due to or associated with, Rh, isoimmunizationP55.0
- newborn, due to or associated with, specified cause NECP59.8
- newborn, due to or associated with, swallowed maternal bloodP58.5
- newborn, spherocytosis (congenital)D58.0
- neonatalSee Jaundice, newborn
- nonhemolytic congenital familial (Gilbert)E80.4
- nuclear, newbornP57.9
- obstructiveK83.1
- post-immunizationSee Hepatitis, viral, type, B
- post-transfusionSee Hepatitis, viral, type, B
- regurgitationK83.1
- serum (homologous) (prophylactic) (therapeutic)See Hepatitis, viral, type, B
- spirochetal (hemorrhagic)A27.0
- symptomaticR17
- symptomatic, newbornP59.9