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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 preterm delivery (due to) 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 newborn P57.9
    obstructive --see also Obstruction, bile duct K83.1
    post-immunization --see Hepatitis, viral, type, B
    post-transfusion --see Hepatitis, viral, type, B
    regurgitation --see also Obstruction, bile duct K83.1
    serum (homologous) (prophylactic) (therapeutic) --see Hepatitis, viral, type, B
    spirochetal (hemorrhagic) A27.0
    symptomatic R17
        newborn P59.9