ICD-10-CM Alphabetic Index · FY 2026 95 Entries

Jaundice in the ICD-10-CM Index ICD-10-CM

The main term Jaundice (yellow) carries 95 index entries pointing to 36 ICD-10-CM codes. The default entry is R17, the code the bare main term maps to; every indented line below refines the term by site, cause, or type. Verify any candidate code in the Tabular List before using it.

✓ Built from the official CMS FY 2026 index fileEffective Oct 1, 2025 – Sep 30, 2026
95
Index Entries
36
Codes Referenced
R17
Default Code
J
Letter
95 of 95 shown
ICD-10-CM

Index Entries Under Jaundice 95 entries · 36 codes

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

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Source: Centers for Medicare & Medicaid Services, FY 2026 ICD-10-CM Index to Diseases and Injuries release files, effective October 1, 2025 through September 30, 2026.