P91.811
BillableNeonatal encephalopathy in diseases classified elsewhere
Neonatal encephalopathy in diseases classified elsewhere
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
- Hyperglycinaemia64654004
- Hyperglycinemia64654004
- Autoimmune thyroiditis66944004
- Cortical blindness68574006
- Disorder of glutamine metabolism190724004
- Disturbance of glutamine metabolism190724004
- Disorder of glycine cleavage enzyme complex237939006
- NKH - Non-ketotic hyperglycinaemia237939006
- NKH - Non-ketotic hyperglycinemia237939006
- Non ketotic hyperglycinaemia237939006
- Non ketotic hyperglycinemia237939006
- Non-ketotic hyperglycinaemia237939006
- Non-ketotic hyperglycinemia237939006
- Infantile epileptic dyskinetic encephalopathy771223000
- Hashimoto encephalitis771271000
- SREAT - steroid-responsive encephalopathy associated with autoimmune thyroiditis771271000
- Steroid-responsive encephalopathy associated with autoimmune thyroiditis771271000
- Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome773548008
- Epilepsy, cortical blindness, intellectual disability, facial dysmorphism syndrome773548008
- KCNQ2 developmental and epileptic encephalopathy778001003
- KCNQ2-DEE - KCNQ2-developmental and epileptic encephalopathy778001003
- KCNQ2-DEE - potassium voltage-gated channel subfamily Q member 2 developmental and epileptic encephalopathy778001003
- Potassium voltage-gated channel subfamily Q member 2 developmental and epileptic encephalopathy778001003
- Neonatal glycine encephalopathy1156803005
- Neonatal non-ketotic hyperglycinaemia1156803005
- Neonatal non-ketotic hyperglycinemia1156803005
- Infantile glycine encephalopathy1156826003
- Infantile non-ketotic hyperglycinaemia1156826003
- Infantile non-ketotic hyperglycinemia1156826003
- Neonatal epileptic encephalopathy due to deficiency of glutaminase1222662000
- Neonatal epileptic encephalopathy due to glutaminase deficiency1222662000
- EIDEE - Early infantile developmental and epileptic encephalopathy721251000124100
- Early infantile developmental and epileptic encephalopathy721251000124100
- Early infantile epileptic encephalopathy721251000124100
- Neonatal metabolic acidaemia16068331000119102
- Neonatal metabolic acidemia16068331000119102
Frequently Asked Questions
What is the ICD-10 code for neonatal encephalopathy in diseases classified elsewhere?
The ICD-10-CM code for neonatal encephalopathy in diseases classified elsewhere is P91.811. The full clinical description is "Neonatal encephalopathy in diseases classified elsewhere". P91.811 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code P91.811 mean?
ICD-10-CM code P91.811 represents "Neonatal encephalopathy in diseases classified elsewhere". 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 P91.811 a billable code?
Yes, P91.811 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P91.811 in?
P91.811 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What SNOMED CT codes does P91.811 map to?
P91.811 maps to 14 SNOMED CT concepts: 66944004, 68574006, 190724004, 237939006, 721251000124100, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P91.811?
P91.811 is linked to 1 UMLS Concept Unique Identifier: C4509426. 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.