Psychogenic movement disorders
Synonyms: Psychogenic dystonia
- Type
- Clinical syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Elderly
- Status
- active
A rare neurologic disease characterized by the manifestation of an underlying psychiatric illness or malingering, and that cannot be attributed to any known structural or neurochemical diseases. Most cases fall in the psychiatric diagnostic category of conversion disorder, also referred to as functional neurological symptom disorder.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Psychogenic movement disorders | Psychogenic dystonia |
| fr | Mouvements anormaux psychogènes | Dystonie psychogène |
| de | Psychogene Bewegungsstörungen | Dystonie, psychogene |
| es | Trastornos del movimiento psicógenos | |
| it | Disturbi psicogeni del movimento | Distonia psicogena |
| nl | Psychogene bewegingsstoornissen | Psychogene dystonie |
| pt | Alterações do movimento psicogénicas | Distonia psicogénica |
| pl | Psychogenne zaburzenia ruchu | Dystonia psychogenna |
| cs | Psychogenní poruchy hybnosti | Psychogenní dystonie |
| uk | Психогенні рухові розлади | Психогенна дистонія |
| zh | 心因性运动障碍 | 心因性肌张力障碍 |
| tr | Psikojenik hareket bozuklukları | Psikojenik distoni |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | F44.4 | NTBT | attributed | validated |
| ICD-11 | 8A0Y | NTBT | index | validated |
| MONDO | 0019114 | E | validated | |
| UMLS | C0752208 | E | validated | |
| MedDRA | 10072376 | 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:102003Rare movement disorder
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET_[EXPERT] |
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
3 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0100022 | Abnormality of movement | |
| Frequent (79-30%) | ||
| HP:0002167 | Abnormality of speech or vocalization | |
| HP:0001288 | Gait disturbance | |
Run the differential on the 1 obligate / very frequent terms
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/71519
- This record as JSON: /data/d/71519.json