• Jaccoud's syndrome M12.0
• Jacksonian epilepsy or seizures (focal) G40.1
• Jackson's
• membrane or veil Q43.3
• paralysis (syndrome) G83.8
• Jacquet's dermatitis L22
• Jadassohn-Pellizari's disease or anetoderma L90.2
• Jadassohn's
• blue nevus Nevus, by site D22.9
• intraepidermal epithelioma Neoplasm, skin, benign
• Jaffe-Lichtenstein(-Uehlinger) syndrome M85.0
• Jakob-Creutzfeldt disease or syndrome A81.0
• with dementia A81.0† F02.1*
• Jaksch-Luzet disease D64.8
• Janet's disease F48.8
• Janiceps Q89.4
• Jansky-Bielschowsky amaurotic idiocy E75.4
• Jaundice (yellow) R17
• acholuric (familial) (splenomegalic) Spherocytosis D58.0
• acquired D59.8
• breast-milk (inhibitor) P59.3
• due to or associated with
• delayed conjugation P59.8
• associated with preterm delivery P59.0
• preterm delivery P59.0
• epidemic (catarrhal)
• leptospiral A27.0
• spirochetal A27.0
• familial nonhemolytic (congenital) (Gilbert) E80.4
• Crigler-Najjar E80.5
• fetus or newborn (physiological) 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
• bruising P58.0
• Crigler-Najjar syndrome E80.5
• delayed conjugation P59.8
• associated with preterm delivery P59.0
• drugs or toxins
• given to newborn P58.4
• transmitted from mother P58.4
• excessive hemolysis NEC P58.9
• specified type NEC P58.8
• galactosemia E74.2
• Gilbert's syndrome E80.4
• hepatocellular damage P59.2
• hereditary hemolytic anemia D58.9
• hypothyroidism, congenital E03.1
• incompatibility, maternal/fetal NEC P55.9
• infection P58.2
• inspissated bile syndrome P59.1
• isoimmunization NEC P55.9
• mucoviscidosis E84.8
• polycythemia P58.3
• preterm delivery P59.0
• Rh
• antibodies P55.0
• incompatibility, maternal/fetal P55.0
• isoimmunization P55.0
• swallowed maternal blood P58.5
• specified cause NEC P59.8
• hematogenous D59.9
• hemolytic (acquired) D59.9
• congenital Spherocytosis D58.0
• hemorrhagic leptosprial (acute) (spirochetal) A27.0
• leptospiral (hemorrhagic) A27.0
• malignant Failure, hepatic K72.9
• neonatal Jaundice, fetus or newborn
• nonhemolytic congenital familial (Gilbert) E80.4
• nuclear, newborn Kernicterus of newborn P57.9
• obstructive Obstruction, bile duct K83.1
• post-immunization Hepatitis, viral, by type B19.-
• post-transfusion Hepatitis, viral, by type B19.-
• regurgitation Obstruction, bile duct K83.1
• serum (homologous) (prophylactic) (therapeutic) Hepatitis, viral, by type
• spirochetal (hemorrhagic) A27.0
• Jaw - see condition
• Jaw-winking phenomenon or syndrome Q07.8
• Jealousy
• alcoholic F10.5
• childhood F93.8
• sibling F93.3
• Jejunitis Enteritis A09.9
• infectious A09.0
• noninfectious K52.9
• Jejunum, jejunal - see condition
• Jensen's disease H30.0
• Jerks, myoclonic G25.3
• Jervell and Lange-Nielsen syndrome I45.8
• Jeune's disease Q77.2
• Jigger disease B88.1
• Joint - see also condition
• mice M24.0
• knee M23.4
• Jüngling's disease Sarcoidosis D86.9
• Juvenile - see condition