P83.2
BillableHydrops fetalis not due to hemolytic disease
Hydrops fetalis not due to hemolytic disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hydrops fetalis NOS
Includes
Conditions included under this code
- conditions that have their origin in the fetal or perinatal period (before birth through the first 28 days after birth) even if morbidity occurs later
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- tetanus neonatorum (A33)
- cradle cap (L21.0)
- diaper [napkin] dermatitis (L22)
Also Known As / Clinical Terms
SNOMED CT
- Edema neonatorum78913002
- Edema of newborn78913002
- Oedema neonatorum78913002
- Oedema of newborn78913002
- Fetal acidosis240306004
- Foetal acidosis240306004
- Generalised oedema271808008
- Generalized edema271808008
- HF - Hydrops fetalis276508000
- HF - Hydrops foetalis276508000
- Hydrops fetalis276508000
- Hydrops foetalis276508000
- Fetal metabolic disorder363204006
- Metabolic disorder of fetus363204006
- Anasarca442433009
- Fetal anaemia462166006
- Fetal anemia462166006
- Foetal anaemia462166006
- Hydros in neonate not due to isoimmunisation713204000
- Hydros in neonate not due to isoimmunization713204000
- Hydros in newborn not due to isoimmunisation713204000
- Hydros in newborn not due to isoimmunization713204000
- Non immune hydrops in newborn713204000
- Non-immune hydrops in neonate713204000
- EPHB4-related generalised lymphatic dysplasia with atrial septal defect1222666002
- EPHB4-related generalised lymphatic dysplasia with non-immune hydrops fetalis1222666002
- EPHB4-related generalized lymphatic dysplasia with atrial septal defect1222666002
- EPHB4-related generalized lymphatic dysplasia with non-immune hydrops fetalis1222666002
- EPHB4-related lymphatic-related hydrops fetalis1222666002
- Ephrin receptor B4-related lymphatic-related hydrops fetalis1222666002
- Generalised lymphatic dysplasia of Fotiou1222667006
- Generalized lymphatic dysplasia of Fotiou1222667006
- PIEZO1-related generalised lymphatic dysplasia with non-immune hydrops fetalis1222667006
- PIEZO1-related generalised lymphatic dysplasia with systemic involvement1222667006
- PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis1222667006
- PIEZO1-related generalized lymphatic dysplasia with systemic involvement1222667006
- PIEZO1-related lymphatic-related hydrops fetalis1222667006
- Piezo type mechanosensitive ion channel component 1-related generalised lymphatic dysplasia with non-immune hydrops fetalis1222667006
- Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis1222667006
- Hydrops, lactic acidosis, sideroblastic anaemia, multisystemic failure syndrome1237349008
- Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome1237349008
UMLS
- Edema, FetalC0020305
- Fetal EdemaC0020305
- Fetal HydropsC0020305
- Fetal edemaC0020305
- Fetal hydropsC0020305
- HF - Hydrops fetalisC0020305
- HF - Hydrops foetalisC0020305
- Hydrops FetalisC0020305
- Hydrops fetalisC0020305
- Hydrops fetalis (disorder)C0020305
- Hydrops fetalis NOSC0020305
- Hydrops foetalisC0020305
- Hydrops, FetalC0020305
- fetal edemaC0020305
- fetal hydropsC0020305
- fetalis hydropsC0020305
- hydrops fetalC0020305
- hydrops fetalisC0020305
- hydrops foetalisC0020305
- Hydrops fetalis not due to hemolytic diseaseC0495455
Frequently Asked Questions
What is the ICD-10 code for hydrops fetalis not due to hemolytic disease?
The ICD-10-CM code for hydrops fetalis not due to hemolytic disease is P83.2. The full clinical description is "Hydrops fetalis not due to hemolytic disease". P83.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code P83.2 mean?
ICD-10-CM code P83.2 represents "Hydrops fetalis not due to hemolytic disease". It is classified under Chapter 16: Certain Conditions Originating in the Perinatal Period and is a billable/specific code that can be used on a claim.
Is P83.2 a billable code?
Yes, P83.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P83.2 in?
P83.2 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What codes cannot be used with P83.2?
P83.2 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital malformations of skin and integument (Q80-Q84); hydrops fetalis due to hemolytic disease (P56.-); neonatal skin infection (P39.4); and 1 more.
What SNOMED CT codes does P83.2 map to?
P83.2 maps to 11 SNOMED CT concepts: 442433009, 1222666002, 78913002, 240306004, 462166006, and 6 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P83.2?
P83.2 is linked to 2 UMLS Concept Unique Identifiers: C0020305, C0495455. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.