1. 2018/2019 ICD-10-CM Index
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Index Terms Starting With 'J' (32) ›

• Jaccoud's syndrome - see Arthropathy, postrheumatic, chronic
• Jackson's
• Jacquet's dermatitis L22
  (diaper dermatitis)
  ICD-10-CM Diagnosis Code L22

  Diaper dermatitis

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Diaper erythema
  • Diaper rash
  • Psoriasiform diaper rash
• Jadassohn's
• Jadassohn-Pellizari's disease or anetoderma L90.2
  ICD-10-CM Diagnosis Code L90.2

  Anetoderma of Jadassohn-Pellizzari

  2016 2017 2018 2019 Billable/Specific Code
• Jaffe-Lichtenstein (-Uehlinger) - see Dysplasia, fibrous, bone NEC
• Jakob-Creutzfeldt disease or syndrome - see Creutzfeldt-Jakob disease or syndrome
• Jaksch-Luzet disease D64.89
  ICD-10-CM Diagnosis Code D64.89

  Other specified anemias

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Infantile pseudoleukemia
• Jamaican
• Janet's disease F48.8
  ICD-10-CM Diagnosis Code F48.8

  Other specified nonpsychotic mental disorders

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Dhat syndrome
  • Neurasthenia
  • Occupational neurosis, including writer's cramp
  • Psychasthenia
  • Psychasthenic neurosis
  • Psychogenic syncope
• Janiceps Q89.4
  ICD-10-CM Diagnosis Code Q89.4

  Conjoined twins

  2016 2017 2018 2019 Billable/Specific Code POA Exempt

  Applicable To

  • Craniopagus
  • Dicephaly
  • Pygopagus
  • Thoracopagus
• Jansky-Bielschowsky amaurotic idiocy E75.4
  ICD-10-CM Diagnosis Code E75.4

  Neuronal ceroid lipofuscinosis

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Batten disease
  • Bielschowsky-Jansky disease
  • Kufs disease
  • Spielmeyer-Vogt disease
• Japanese
• Jaundice (yellow) R17
  ICD-10-CM Diagnosis Code R17

  Unspecified jaundice

  2016 2017 2018 2019 Billable/Specific Code

  Type 1 Excludes

  • neonatal jaundice (P55, P57-P59)
• Jaw - see condition
• Jaw-winking phenomenon or syndrome Q07.8
  ICD-10-CM Diagnosis Code Q07.8

  Other specified congenital malformations of nervous system

  2016 2017 2018 2019 Billable/Specific Code POA Exempt

  Applicable To

  • Agenesis of nerve
  • Displacement of brachial plexus
  • Jaw-winking syndrome
  • Marcus Gunn's syndrome
• Jealousy
• Jejunitis - see Enteritis
• Jejunostomy status Z93.4
  ICD-10-CM Diagnosis Code Z93.4

  Other artificial openings of gastrointestinal tract status

  2016 2017 2018 2019 Billable/Specific Code POA Exempt
• Jejunum, jejunal - see condition
• Jensen's disease - see Inflammation, chorioretinal, focal, juxtapapillary
• Jerks, myoclonic G25.3
  ICD-10-CM Diagnosis Code G25.3

  Myoclonus

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Drug-induced myoclonus
  • Palatal myoclonus

  Type 1 Excludes

  • facial myokymia (G51.4)
  • myoclonic epilepsy (G40.-)

  Use Additional

  • code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
• Jervell-Lange-Nielsen syndrome I45.81
  ICD-10-CM Diagnosis Code I45.81

  Long QT syndrome

  2016 2017 2018 2019 Billable/Specific Code
• Jeune's disease Q77.2
  ICD-10-CM Diagnosis Code Q77.2

  Short rib syndrome

  2016 2017 2018 2019 Billable/Specific Code POA Exempt

  Applicable To

  • Asphyxiating thoracic dysplasia [Jeune]
• Jigger disease B88.1
  ICD-10-CM Diagnosis Code B88.1

  Tungiasis [sandflea infestation]

  2016 2017 2018 2019 Billable/Specific Code
• Job's syndrome D71
  (chronic granulomatous disease)
  ICD-10-CM Diagnosis Code D71

  Functional disorders of polymorphonuclear neutrophils

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Cell membrane receptor complex [CR3] defect
  • Chronic (childhood) granulomatous disease
  • Congenital dysphagocytosis
  • Progressive septic granulomatosis
• Joint - see also condition
• Jordan's anomaly or syndrome D72.0
  ICD-10-CM Diagnosis Code D72.0

  Genetic anomalies of leukocytes

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Alder (granulation) (granulocyte) anomaly
  • Alder syndrome
  • Hereditary leukocytic hypersegmentation
  • Hereditary leukocytic hyposegmentation
  • Hereditary leukomelanopathy
  • May-Hegglin (granulation) (granulocyte) anomaly
  • May-Hegglin syndrome
  • Pelger-Huët (granulation) (granulocyte) anomaly
  • Pelger-Huët syndrome

  Type 1 Excludes

  • Chédiak (-Steinbrinck)-Higashi syndrome (E70.330)
• Joseph-Diamond-Blackfan anemia D61.01
  (congenital hypoplastic)
  ICD-10-CM Diagnosis Code D61.01

  Constitutional (pure) red blood cell aplasia

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Blackfan-Diamond syndrome
  • Congenital (pure) red cell aplasia
  • Familial hypoplastic anemia
  • Primary (pure) red cell aplasia
  • Red cell (pure) aplasia of infants

  Type 1 Excludes

  • acquired red cell aplasia (D60.9)
• Jungle yellow fever A95.0
  ICD-10-CM Diagnosis Code A95.0

  Sylvatic yellow fever

  2016 2017 2018 2019 Billable/Specific Code

  Applicable To

  • Jungle yellow fever
• Jüngling's disease - see Sarcoidosis
• Juvenile - see condition