Idiopathic catatonia
Synonyms: Idiopathic catatonic syndrome · Isolated catatonia · Isolated catatonic syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare neurologic disease with psychiatric involvement characterized by a cluster of signs and symptoms of catatonia that is not associated with any underlying psychiatric or organic disorder or intoxication.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic catatonia | Idiopathic catatonic syndrome · Isolated catatonia · Isolated catatonic syndrome |
| fr | Catatonie idiopathique | Catatonie isolée · Syndrome catatonique idiopathique · Syndrome catatonique isolé |
| de | Idiopathische Katatonie | |
| es | Catatonía idiopática | |
| it | Catatonia idiopatica | |
| nl | Idiopathische katatonie | |
| pt | Catatonia idiopática | |
| pl | Idiopatyczna katatonia | = en |
| cs | Idiopatická katatonie | = en |
| uk | Ідіопатична кататонія | Ідіопатичний кататонічний синдром · Ізольована кататонія · Ізольований кататонічний синдром |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | F20.2 | NTBT | attributed | validated |
| MONDO | 0957487 | E | validated | |
| UMLS | C5816742 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98033Rare neurologic disease with psychiatric involvement
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 16 cases | Worldwide | Case(s) | Validated | 26243853[PMID]_37138368[PMID]_36649557[PMID]_23051079[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 26243853[PMID]_37138368[PMID]_36649557[PMID]_23051079[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.
HPO phenotypes
16 annotations · validated 2025-03-04| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0002533 | Abnormal posturing | |
| HP:0000733 | Abnormal repetitive mannerisms | |
| HP:0000713 | Agitation | |
| HP:0002039 | Anorexia | |
| HP:0007302 | Bipolar affective disorder | |
| HP:0001259 | Coma | |
| HP:0010529 | Echolalia | |
| HP:0000273 | Facial grimacing | |
| HP:0002300 | Mutism | |
| HP:0410291 | Negativism | |
| HP:0100753 | Schizophrenia | |
| Occasional (29-5%) | ||
| HP:0002396 | Cogwheel rigidity | |
| HP:0030903 | Grasp reflex | |
| HP:0000752 | Hyperactivity | |
| HP:0100710 | Impulsivity | |
| HP:0025401 | Staring gaze | |
Annotation source: 37523662[PMID]_28613592[PMID]_26243853[PMID]_17558626[PMID]_25538636[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/648919
- This record as JSON: /data/d/648919.json