P91.819
BillableNeonatal encephalopathy, unspecified
Neonatal encephalopathy, unspecified
Coding Notes
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 2
Conditions not included here, but the patient may have both
Also Known As / Clinical Terms
SNOMED CT
- Axonal neuropathy60703000
- Neonatal encephalopathy95628005
- Hypertrophic mitochondrial cardiomyopathy472316006
- Coenzyme Q10 deficiency724575009
- Epileptic encephalopathy with global cerebral demyelination726702005
- Mitochondrial aspartate-glutamate carrier 1 deficiency726702005
- Bonnemann Meinecke Reich syndrome733049004
- Encephalopathy, intracerebral calcification, retinal degeneration syndrome733049004
- SCN8A developmental and epileptic encephalopathy765170001
- SCN8A-DEE - SCN8A - developmental and epileptic encephalopathy765170001
- SCN8A-DEE - sodium voltage-gated channel alpha subunit 8 developmental and epileptic encephalopathy765170001
- Sodium voltage-gated channel alpha subunit 8 developmental and epileptic encephalopathy765170001
- MECP2-related severe neonatal encephalopathy771303004
- Severe congenital encephalopathy due to MECP2 (methyl-CpG binding protein 2) mutation771303004
- Severe congenital encephalopathy due to MECP2 mutation771303004
- Severe congenital encephalopathy due to methyl-CpG binding protein 2 mutation771303004
- Severe neonatal onset encephalopathy with microcephaly771303004
- SCN2A encephalopathy778002005
- Sodium voltage-gated channel alpha subunit 2 encephalopathy778002005
- Myoclonic epilepsy in non-progressive encephalopathy778047006
- COQ4-related neonatal encephalomyopathy1186718008
- Coenzyme Q4-related neonatal encephalomyopathy1186718008
- Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome1186718008
- Lethal neonatal rigidity, multifocal seizure syndrome1197587003
- Lethal neonatal spasticity, epileptic encephalopathy syndrome1197587003
- CNTNAP2 developmental and epileptic encephalopathy1230376005
- CNTNAP2-DEE - CNTNAP2 developmental and epileptic encephalopathy1230376005
- CNTNAP2-related developmental and epileptic encephalopathy1230376005
- Contactin associated protein 2-related developmental and epileptic encephalopathy1230376005
- Cortical dysplasia, focal epilepsy syndrome1230376005
- Congenital axonal neuropathy with encephalopathy1237626001
- MECP2 (methyl-cytosine phosphate guanine binding protein-2) disorder1296869000
- MECP2 related disorder1296869000
- Methyl-CpG (cytosine phosphate guanine) binding protein-2 disorder1296869000
- Methyl-CpG binding protein 2 related disorder1296869000
- Methyl-cytosine phosphate guanine binding protein-2 related disorder1296869000
- Encephalopathy due to COVID-191240561000000108
- Encephalopathy due to disease caused by 2019 novel coronavirus1240561000000108
- Encephalopathy due to disease caused by 2019-nCoV1240561000000108
- Encephalopathy due to disease caused by SARS-CoV-21240561000000108
- Encephalopathy due to disease caused by severe acute respiratory syndrome coronavirus 21240561000000108
Frequently Asked Questions
What is the ICD-10 code for neonatal encephalopathy, unspecified?
The ICD-10-CM code for neonatal encephalopathy, unspecified is P91.819. The full clinical description is "Neonatal encephalopathy, unspecified". P91.819 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code P91.819 mean?
ICD-10-CM code P91.819 represents "Neonatal encephalopathy, unspecified". 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 P91.819 a billable code?
Yes, P91.819 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P91.819 in?
P91.819 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What SNOMED CT codes does P91.819 map to?
P91.819 maps to 16 SNOMED CT concepts: 60703000, 733049004, 1230376005, 1186718008, 724575009, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P91.819?
P91.819 is linked to 1 UMLS Concept Unique Identifier: C4509427. 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.