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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 2020 2021 2022 2023 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 2020 2021 2022 2023 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 2020 2021 2022 2023 Billable/Specific Code
-
Jamaican
-
Janet's disease F48.8
ICD-10-CM Diagnosis Code F48.8
Other specified nonpsychotic mental disorders
2016 2017 2018 2019 2020 2021 2022 2023 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 2020 2021 2022 2023 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 2020 2021 2022 2023 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 2020 2021 2022 2023 Billable/Specific Code
-
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 2020 2021 2022 2023 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 2020 2021 2022 2023 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 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Drug-induced myoclonus
- Palatal myoclonus
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 2020 2021 2022 2023 Billable/Specific Code
-
Jeune's disease Q77.2
ICD-10-CM Diagnosis Code Q77.2
Short rib syndrome
2016 2017 2018 2019 2020 2021 2022 2023 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 2020 2021 2022 2023 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 2020 2021 2022 2023 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 2020 2021 2022 2023 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 2020 2021 2022 2023 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 2020 2021 2022 2023 Billable/Specific Code
-
Jüngling's disease - see Sarcoidosis
-
Juvenile - see condition