P90
BillableConvulsions of newborn
Convulsions of newborn
Status
Billable / Specific
Block
P90-P96
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 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
Also Known As / Clinical Terms
SNOMED CT
- SeLNE - self-limited neonatal epilepsy38281008
- Self-limited neonatal epilepsy38281008
- Choreoathetosis43105007
- EEG abnormality with seizure43400009
- Electroencephalogram abnormality with seizure43400009
- Neonatal diabetes mellitus49817004
- Paroxysmal choreoathetosis49949003
- Paroxysmal dyskinesia49949003
- Central convulsion58895005
- Essential convulsion58895005
- Spontaneous convulsion58895005
- Tetanic convulsion71587006
- Epileptic cry73706008
- Neonatal seizure87476004
- Convulsion91175000
- Fit91175000
- Fit - convulsion91175000
- Fitting91175000
- Seizure91175000
- Seizure disorder128613002
- Situation-related seizures230431001
- Disorder of lysine and hydroxylysine metabolism237929000
- Lysine and hydroxylysine metabolism disorder237929000
- Disorder of beta and omega amino acid metabolism237940008
- Epilepsy monitoring status243857008
- Seizures complicating intracranial haemorrhage in the newborn371107004
- Seizures complicating intracranial hemorrhage in the newborn371107004
- Seizures complicating intracranial haemorrhage371114002
- Seizures complicating intracranial hemorrhage371114002
- Seizures complicating infection371115001
- Seizures complicating infection in the newborn372441001
- Daily seizures407621003
- Many seizures a day407622005
- Emergency epilepsy treatment since last appointment407623000
- Paroxysmal kinesigenic choreoathetosis609221008
- Paroxysmal kinesigenic dyskinesia609221008
- ICCA syndrome715534008
- Infantile convulsion and choreoathetosis syndrome715534008
- Paroxysmal kinesigenic dyskinesia and infantile convulsion715534008
- Folinic acid responsive seizures717276003
- Folinic acid responsive developmental and epileptic encephalopathy717276003
- DEND (developmental delay, epilepsy, neonatal diabetes) syndrome721088003
- DEND syndrome721088003
- Developmental delay, epilepsy, neonatal diabetes syndrome721088003
- Seizures and intellectual disability due to hydroxylysinuria723994004
- Seizures and intellectual disability due to hydroxylysinuria syndrome723994004
- Seizure co-occurrent and due to sedative withdrawal724668002
- Seizure co-occurrent and due to psychoactive substance withdrawal724727001
- Antiquitin deficiency734434007
- PD-DEE - pyridoxine-dependent developmental and epileptic encephalopathy734434007
- Pyridoxine-dependent DEE (developmental and epileptic encephalopathy)734434007
- Pyridoxine-dependent developmental and epileptic encephalopathy734434007
- Pyridoxine-dependent epilepsy734434007
- Vitamin B6-dependent seizures734434007
- Intellectual disability, seizures, macrocephaly, obesity syndrome770750002
- Congenital disorder of glycosylation due to PIGT (phosphatidylinositol glycan anchor biosynthesis class T) deficiency770755007
- Congenital disorder of glycosylation due to PIGT deficiency770755007
- Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome770755007
- MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3770755007
- Primary hyperaldosteronism, seizures, neurological abnormalities syndrome789063000
- Acute seizure due to infection of central nervous system838351006
- Lethal neonatal rigidity, multifocal seizure syndrome1197587003
- Lethal neonatal spasticity, epileptic encephalopathy syndrome1197587003
- GPAA1-related biosynthesis defect1217381009
- Glycosylphosphatidylinositol anchor attachment 1-related biosynthesis defect1217381009
- Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome1217381009
- Seizure co-occurrent and due to substance withdrawal1254960008
- Ictal traumatic injury1263508001
- Traumatic injury due to seizure1263508001
- Neonatal epileptic seizure1287613001
- Neonatal focal epileptic seizure1287613001
- Neonatal electro-clinical epileptic seizure1287614007
- Neonatal electro-clinical seizure1287614007
- Neonatal focal electro-clinical epileptic seizure1287614007
- Neonatal electrographic-only seizure1287615008
- Neonatal focal electrographic-only epileptic seizure1287615008
- Neonatal focal non-motor electro-clinical epileptic seizure1287616009
- Neonatal non-motor electro-clinical seizure1287616009
- Neonatal non-motor seizure1287616009
- Neonatal nonmotor electro-clinical seizure1287616009
- Neonatal focal motor electro-clinical epileptic seizure1287617000
- Neonatal motor electro-clinical seizure1287617000
- Neonatal motor seizure1287617000
- Neonatal focal sequential electro-clinical epileptic seizure1287618005
- Neonatal sequential electro-clinical seizure1287618005
- Neonatal sequential seizure1287618005
- Neonatal automatism seizure1287619002
- Neonatal focal automatism epileptic seizure1287619002
- Neonatal focal myoclonic epileptic seizure1287620008
- Neonatal myoclonic seizure1287620008
- Neonatal focal tonic epileptic seizure1287621007
- Neonatal tonic seizure1287621007
- Neonatal clonic seizure1287622000
- Neonatal focal clonic epileptic seizure1287622000
- Neonatal epileptic spasms1287623005
- Neonatal focal epileptic spasms1287623005
- Neonatal autonomic seizure1287624004
- Neonatal focal autonomic epileptic seizure1287624004
- Neonatal behavioral arrest seizure1287625003
- Neonatal behavioural arrest seizure1287625003
- Neonatal focal behavioral arrest epileptic seizure1287625003
- Neonatal focal behavioural arrest epileptic seizure1287625003
- Genetic syndromic childhood obesity1359763002
- Acute repetitive seizure460681000124100
- Cluster seizure460681000124100
- Crescendo seizure460681000124100
- Serial seizure460681000124100
- Disorder of GABA (gamma aminobutyric acid) metabolism16909721000119103
- Disorder of gamma aminobutyric acid metabolism16909721000119103
- Disorder of gamma-aminobutyric acid metabolism16909721000119103
- Hereditary cerebellar atrophy431641000124107
- Recurrent seizure460731000124105
UMLS
- Convulsion neonatalC0159020
- Convulsions in newbornC0159020
- Convulsions neonatalC0159020
- Convulsions of newbornC0159020
- Neonatal SeizureC0159020
- Neonatal convulsionC0159020
- Neonatal fitC0159020
- Neonatal seizureC0159020
- Neonatal seizure (finding)C0159020
- Neonatal seizuresC0159020
- neonatal convulsionC0159020
- neonatal convulsionsC0159020
- neonatal seizureC0159020
- neonatal seizuresC0159020
- newborn seizureC0159020
- newborn seizuresC0159020
- newborns seizureC0159020
- newborns seizuresC0159020
- seizure newbornC0159020
- seizures in newbornC0159020
- seizures newbornC0159020
Frequently Asked Questions
What is ICD-10 code P90?
ICD-10-CM code P90 represents "Convulsions of newborn". It is a billable/specific code that can be used on a claim.
Is P90 a billable code?
Yes, P90 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P90 in?
P90 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What codes cannot be used with P90?
P90 has Excludes1 notes indicating codes that cannot be used together with it, including: benign myoclonic epilepsy in infancy (G40.3-); benign neonatal convulsions (familial) (G40.3-).
What SNOMED CT codes does P90 map to?
P90 maps to 56 SNOMED CT concepts: 717276003, 460681000124100, 838351006, 734434007, 58895005, and 51 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P90?
P90 is linked to 1 UMLS Concept Unique Identifier: C0159020. 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.