| J |
| Jaccoud's syndrome --see Arthropathy, postrheumatic, chronic |
| Jackson's |
| membrane Q43.3 |
| paralysis or syndrome G83.89 |
| veil Q43.3 |
| Jacquet's dermatitis(diaper dermatitis) L22 |
| Jadassohn-Pellizari's disease or anetoderma L90.2 |
| Jadassohn's |
| blue nevus --see Nevus |
| intraepidermal epithelioma --see Neoplasm, skin, benign |
| Jaffe-Lichtenstein(-Uehlinger) syndrome --see Dysplasia, fibrous, bone NEC |
| Jakob-Creutzfeldt disease or syndrome --see Creutzfeldt-Jakob disease or syndrome |
| Jaksch-Luzet disease D64.89 |
| Jamaican |
| neuropathy G92 |
| paraplegic tropical ataxic-spastic syndrome G92 |
| Janet's disease F48.8 |
| Janiceps Q89.4 |
| Jansky-Bielschowsky amaurotic idiocy E75.4 |
| Japanese |
| B-type encephalitis A83.0 |
| river fever A75.3 |
| 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(due to) preterm delivery 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 newbornP57.9 |
| obstructive --see also Obstruction, bile ductK83.1 |
| post-immunization --see Hepatitis, viral, type, B |
| post-transfusion --see Hepatitis, viral, type, B |
| regurgitation --see also Obstruction, bile ductK83.1 |
| serum(homologous) (prophylactic) (therapeutic) --see Hepatitis, viral, type, B |
| spirochetal(hemorrhagic) A27.0 |
| symptomatic R17 |
| newborn P59.9 |
| Jaw --see condition |
| Jaw-winking phenomenon or syndrome Q07.8 |
| Jealousy |
| alcoholic F10.988 |
| childhood F93.8 |
| sibling F93.8 |
| Jejunitis --see Enteritis |
| Jejunostomy status Z93.4 |
| Jejunum, jejunal --see condition |
| Jensen's disease --see Inflammation, chorioretinal, focal, juxtapapillary |
| Jerks, myoclonic G25.3 |
| Jervell-Lange-Nielsen syndrome I45.81 |
| Jeune's disease Q77.2 |
| Jigger disease B88.1 |
| Job's syndrome(chronic granulomatous disease) D71 |
| Joint --see also condition |
| mice --see Loose, body, joint |
| knee M23.4- |
| Jordan's anomaly or syndrome D72.0 |
| Joseph-Diamond-Blackfan anemia(congenital hypoplastic) D61.01 |
| Jungle yellow fever A95.0 |
| Jüngling's disease --see Sarcoidosis |
| Juvenile --see condition |