Persistent idiopathic facial pain
Synonyms: AFP · Atypical facial pain · PIFP
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare neurological disease characterized by a generally deep, poorly localized, persistent facial pain that does not present characteristics of a cranial neuralgia and which cannot be attributed to another disorder.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Persistent idiopathic facial pain | AFP · Atypical facial pain · PIFP |
| fr | Douleur faciale idiopathique persistante | AFP · Douleur faciale atypique · PIFP |
| de | Persistierender idiopathischer Gesichtsschmerz | AFP · Gesichtsschmerz, atypischer · PIFP |
| es | Dolor facial persistente idiopático | AFP · Dolor facial atípico · PIFP |
| it | Dolore facciale idiopatico persistente | AFP · Dolore facciale atipico · PIFP |
| nl | Persisterende idiopathische aangezichtspijn | AFP · Atypische aangezichtspijn · PIFP |
| pt | Dor facial idiopática persistente | |
| pl | Przetrwały idiopatyczny ból twarzy | AFP · Atypowy ból twarzy · PIFP |
| cs | Perzistentní idiopatická bolest obličeje | AFP · PIFP · Atypická obličejová bolest |
| uk | Постійний ідіопатичний біль обличчя | AFP · Атиповий лицьовий біль · PIFP |
| zh | 持续性特发性面部疼痛 | 非典型性面部疼痛 |
| tr | Kalıcı idiyopatik yüz ağrısı | AFP · PIFP · Atipik fasiyal ağrı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G50.1 | E | specific | validated |
| ICD-11 | 8A85 | NTBT | index | validated |
| MONDO | 0018362 | E | validated | |
| UMLS | C5191641 | 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:98006Rare neurologic disease
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
4 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Lifetime Prevalence | 1-5 / 10 000 | 30 / 100 000 | Germany | Value and class | Validated | 21960648[PMID] |
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
| Annual incidence | 1-9 / 100 000 | 4.4 / 100 000 | Netherlands | Value and class | Validated | 19783099[PMID] |
| Annual incidence | 1-9 / 100 000 | 1 / 100 000 | Germany | Value and class | Validated | 12911872[PMID] |
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
11 annotations · validated 2024-07-10| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0000271 | Abnormality of the face | |
| HP:0012532 | Chronic pain | |
| Frequent (79-30%) | ||
| HP:0025282 | Dull | |
| Occasional (29-5%) | ||
| HP:0003489 | Acute episodes of neuropathic symptoms | |
| HP:0000739 | Anxiety | |
| HP:0032143 | Burning mouth | |
| HP:0000716 | Depression | |
| HP:0007328 | Impaired pain sensation | |
| HP:0003401 | Paresthesia | |
| Very rare (<4-1%) | ||
| HP:0003474 | Somatic sensory dysfunction | |
| Excluded (0%) | ||
| HP:0012639 | Abnormal nervous system morphology | |
Run the differential on the 2 obligate / very frequent terms
Annotation source: 28251523[PMID]_28425324[PMID]_32992770[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/398147
- This record as JSON: /data/d/398147.json