Jaundice (yellow)

"Jaundice (yellow)" References in the ICD-10-CM Index to Diseases and Injuries

References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "jaundice (yellow)"

  • Jaundice (yellow) - R17 Unspecified jaundice
    • acholuric (familial) (splenomegalic) - See Also: Spherocytosis;
      • acquired - D59.8 Other acquired hemolytic anemias
    • breast-milk (inhibitor) - P59.3 Neonatal jaundice from breast milk inhibitor
    • catarrhal (acute) - B15.9 Hepatitis A without hepatic coma
      • with hepatic coma - B15.0 Hepatitis A with hepatic coma
    • cholestatic (benign) - R17 Unspecified jaundice
    • due to or associated with
      • delayed conjugation - P59.8 Neonatal jaundice from other specified causes
        • associated with (due to) preterm delivery - P59.0 Neonatal jaundice associated with preterm delivery
      • preterm delivery - P59.0 Neonatal jaundice associated with preterm delivery
    • epidemic (catarrhal) - B15.9 Hepatitis A without hepatic coma
      • leptospiral - A27.0 Leptospirosis icterohemorrhagica
      • spirochetal - A27.0 Leptospirosis icterohemorrhagica
      • with hepatic coma - B15.0 Hepatitis A with hepatic coma
    • familial nonhemolytic (congenital) (Gilbert) - E80.4 Gilbert syndrome
      • Crigler-Najjar - E80.5 Crigler-Najjar syndrome
    • febrile (acute) - B15.9 Hepatitis A without hepatic coma
      • leptospiral - A27.0 Leptospirosis icterohemorrhagica
      • spirochetal - A27.0 Leptospirosis icterohemorrhagica
      • with hepatic coma - B15.0 Hepatitis A with hepatic coma
    • hematogenous - D59.9 Acquired hemolytic anemia, unspecified
    • hemolytic (acquired) - D59.9 Acquired hemolytic anemia, unspecified
      • congenital - See: Spherocytosis;
    • hemorrhagic (acute) (leptospiral) (spirochetal) - A27.0 Leptospirosis icterohemorrhagica
    • infectious (acute) (subacute) - B15.9 Hepatitis A without hepatic coma
      • leptospiral - A27.0 Leptospirosis icterohemorrhagica
      • spirochetal - A27.0 Leptospirosis icterohemorrhagica
      • with hepatic coma - B15.0 Hepatitis A with hepatic coma
    • leptospiral (hemorrhagic) - A27.0 Leptospirosis icterohemorrhagica
    • malignant (without coma) - K72.90 Hepatic failure, unspecified without coma
      • with coma - K72.91 Hepatic failure, unspecified with coma
    • neonatal - See: Jaundice, newborn;
    • newborn - P59.9 Neonatal jaundice, unspecified
      • due to or associated with
        • ABO
          • antibodies - P55.1 ABO isoimmunization of newborn
          • incompatibility, maternal/fetal - P55.1 ABO isoimmunization of newborn
          • isoimmunization - P55.1 ABO isoimmunization of newborn
        • absence or deficiency of enzyme system for bilirubin conjugation (congenital) - P59.8 Neonatal jaundice from other specified causes
        • bleeding - P58.1 Neonatal jaundice due to bleeding
        • breast milk inhibitors to conjugation - P59.3 Neonatal jaundice from breast milk inhibitor
          • associated with preterm delivery - P59.0 Neonatal jaundice associated with preterm delivery
        • bruising - P58.0 Neonatal jaundice due to bruising
        • Crigler-Najjar syndrome - E80.5 Crigler-Najjar syndrome
        • delayed conjugation - P59.8 Neonatal jaundice from other specified causes
          • associated with preterm delivery - P59.0 Neonatal jaundice associated with preterm delivery
        • drugs or toxins
          • given to newborn - P58.42 Neonatal jaundice due to drugs or toxins given to newborn
          • transmitted from mother - P58.41 Neonatal jaundice due to drugs or toxins transmitted from mother
        • excessive hemolysis - P58.9 Neonatal jaundice due to excessive hemolysis, unspecified
          • due to
            • bleeding - P58.1 Neonatal jaundice due to bleeding
            • bruising - P58.0 Neonatal jaundice due to bruising
            • drugs or toxins
              • given to newborn - P58.42 Neonatal jaundice due to drugs or toxins given to newborn
              • transmitted from mother - P58.41 Neonatal jaundice due to drugs or toxins transmitted from mother
            • infection - P58.2 Neonatal jaundice due to infection
            • polycythemia - P58.3 Neonatal jaundice due to polycythemia
            • swallowed maternal blood - P58.5 Neonatal jaundice due to swallowed maternal blood
          • specified type NEC - P58.8 Neonatal jaundice due to other specified excessive hemolysis
        • galactosemia - E74.21 Galactosemia
        • Gilbert syndrome - E80.4 Gilbert syndrome
        • hemolytic disease - P55.9 Hemolytic disease of newborn, unspecified
          • ABO isoimmunization - P55.1 ABO isoimmunization of newborn
          • Rh isoimmunization - P55.0 Rh isoimmunization of newborn
          • specified NEC - P55.8 Other hemolytic diseases of newborn
        • hepatocellular damage - P59.20 Neonatal jaundice from unspecified hepatocellular damage
          • specified NEC - P59.29 Neonatal jaundice from other hepatocellular damage
        • hereditary hemolytic anemia - P58.8 Neonatal jaundice due to other specified excessive hemolysis
        • hypothyroidism, congenital - E03.1 Congenital hypothyroidism without goiter
        • incompatibility, maternal/fetal NOS - P55.9 Hemolytic disease of newborn, unspecified
        • infection - P58.2 Neonatal jaundice due to infection
        • inspissated bile syndrome - P59.1 Inspissated bile syndrome
        • isoimmunization NOS - P55.9 Hemolytic disease of newborn, unspecified
        • mucoviscidosis - E84.9 Cystic fibrosis, unspecified
        • polycythemia - P58.3 Neonatal jaundice due to polycythemia
        • preterm delivery - P59.0 Neonatal jaundice associated with preterm delivery
        • Rh
          • antibodies - P55.0 Rh isoimmunization of newborn
          • incompatibility, maternal/fetal - P55.0 Rh isoimmunization of newborn
          • isoimmunization - P55.0 Rh isoimmunization of newborn
        • specified cause NEC - P59.8 Neonatal jaundice from other specified causes
        • swallowed maternal blood - P58.5 Neonatal jaundice due to swallowed maternal blood
      • spherocytosis (congenital) - D58.0 Hereditary spherocytosis
    • nonhemolytic congenital familial (Gilbert) - E80.4 Gilbert syndrome
    • nuclear, newborn - See Also: Kernicterus of newborn; - P57.9 Kernicterus, unspecified
    • obstructive - See Also: Obstruction, bile duct; - K83.1 Obstruction of bile duct
    • post-immunization - See: Hepatitis, viral, type, B;
    • post-transfusion - See: Hepatitis, viral, type, B;
    • regurgitation - See Also: Obstruction, bile duct; - K83.1 Obstruction of bile duct
    • serum (homologous) (prophylactic) (therapeutic) - See: Hepatitis, viral, type, B;
    • spirochetal (hemorrhagic) - A27.0 Leptospirosis icterohemorrhagica
    • symptomatic - R17 Unspecified jaundice
      • newborn - P59.9 Neonatal jaundice, unspecified

Applicable Clinical Terms Definitions

Antibodies: Immunoglobulin molecules having a specific amino acid sequence by virtue of which they interact only with the ANTIGEN (or a very similar shape) that induced their synthesis in cells of the lymphoid series (especially PLASMA CELLS).

Crigler-Najjar Syndrome: A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.

Galactosemias: A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)

Infection: Invasion of the host organism by microorganisms that can cause pathological conditions or diseases.

Infant, Newborn: An infant during the first 28 days after birth.

Polycythemia: An increase in the total red cell mass of the blood. (Dorland, 27th ed)