Alphabetic Index · main term

Jaundice (yellow)

FY2027Index: J /Alphabetic Index

At the main termR17

Jaundice (yellow) is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists R17 for the term on its own. It has 94 subterms and 82 code entries. First-level subterms include acholuric, breast-milk, catarrhal, cholestatic, due to or associated with, epidemic, familial nonhemolytic, febrile and more. Confirm any code you find here in the Tabular List before you report it.

Subterms 94

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