raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:641496

Childhood-onset schizophrenia

Synonyms: COS · VEOS · Very early-onset schizophrenia

Type
Disease
Group
Disorder
Inheritance
Multigenic/multifactorial
Age of onset
Adolescent, Childhood
Status
active

A rare neurologic disease with psychiatric involvement characterized by prominent pre-psychotic developmental disabilities (cognitive, language, motor), socio-communicative disturbances, auditory hallucinations (visual and tactile hallucinations are rarer) preceding psychotic symptoms, presenting before 13 years of age. Co-occurrence of neurodevelopmental disorders (e.g. autism spectrum disorders, attention deficit hyperactivity disorder) is frequent. Disease course is more severe than adult-onset form of the disease, with major neurodevelopmental impact.

1

Names in Orphadata languages

10 of 12 languages
LangNameSynonyms
enChildhood-onset schizophreniaCOS · VEOS · Very early-onset schizophrenia
frSchizophrénie à début infantileSDTP
deSchizophrenie im KindesalterSchizophrenie, früh beginnende
esEsquizofrenia de inicio en la infancia
itSchizofrenia ad esordio infantileCOS · Schizofrenia ad esordio molto precoce · VEOS
nlSchizofrenie beginnend op kinderleeftijdCOS · VEOS · Zeer vroeg optredende schizofrenie
ptEsquizofrenia com início na infânciaCOS · Esquizofrenia de início muito precoce · VEOS
plSchizofrenia o początku w wieku dziecięcym= en
csSchizofrenie s nástupem v dětství= en
ukШизофренія з дебютом у дитинствіCOS · VEOS · Дуже рання шизофренія

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10F20.0BTNTattributedvalidated
ICD-10F20.1BTNTattributedvalidated
ICD-10F20.2BTNTattributedvalidated
ICD-10F20.3BTNTattributedvalidated
ICD-10F20.4BTNTattributedvalidated
ICD-10F20.5BTNTattributedvalidated
ICD-10F20.6BTNTattributedvalidated
ICD-10F20.8BTNTattributedvalidated
MONDO0957430Evalidated
MeSHD012561Evalidated
UMLSC0036346Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

Codes that Orphanet moved or referred to this one:

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Annual incidence1-5 / 10 000—EuropeClass onlyValidated22906158[PMID]_ORPHANET
Point prevalenceUnknown—EuropeClass onlyValidated22906158[PMID]_ORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

20 annotations · validated 2026-02-06
HPOTerm (as annotated by Orphanet)Diagnostic
Very frequent (99-80%)
HP:0000709Psychosis
Frequent (79-30%)
HP:0000745Abnormal diminished volition
HP:0007018Attention deficit hyperactivity disorder
HP:0000729Autistic behavior
HP:0100543Cognitive impairment
HP:0000746Delusion
HP:5200310Diminishment of social interactions
HP:0025769Disordered formal thought process
HP:0000738Hallucinations
HP:0033051Impaired executive functioning
HP:0011999Paranoia
Occasional (29-5%)
HP:0033511Addictive substance use
HP:0000716Depression
HP:0006892Frontotemporal cerebral atrophy
HP:0001263Global developmental delay
HP:0006956Lateral ventricle dilatation
HP:0002300Mutism
HP:0031589Suicidal ideation
HP:5200330Suicide behaviors
HP:0025784Word salad

Run the differential on the 1 obligate / very frequent terms

Annotation source: PNDS 2022[OTHER]_30969686[PMID]_38492329[PMID]_39867751[PMID]

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Sources for this card