Phalangeal microgeodic syndrome
Synonyms: Phalangeal osteolysis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Childhood
- Status
- active
A rare primary osteolysis disorder characterized by multiple small osteolytic areas and sclerosis in the phalanges of one or both hands associated with swelling and redness of the phalanges. Condition is benign, self-limited and may be associated with cold exposure.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Phalangeal microgeodic syndrome | Phalangeal osteolysis |
| fr | Syndrome microgéodique des phalanges | Ostéolyse phalangienne |
| de | Transitorische Osteolyse der Phalangen | Phalangeale Osteolyse |
| es | Síndrome falángico microgeódico | Acroosteólisis falángica |
| it | Sindrome microgeodica falangea | Osteolisi falangea |
| nl | Falangeaal microgeodisch syndroom | Falangeale osteolyse |
| pt | Síndrome de falanges micro geodésicas | |
| pl | Phalangeal microgeodic syndrome | Osteoliza paliczków |
| cs | Falangeální osteolýza | Falangeální mikrogeodický syndrom |
| uk | Фаланговий мікрогеодичний синдром | Остеоліз фалангових кісток |
| zh | 指骨小晶洞病综合征 | 指骨溶解症 |
| tr | Falangeal mikrojeodik sendrom | Falanjiyal osteoliz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M89.5 | NTBT | attributed | validated |
| ICD-11 | FB86.2 | NTBT | attributed | validated |
| MONDO | 0018128 | E | validated | |
| UMLS | C4749465 | 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:93449Primary osteolysis
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone 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 | 50 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 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
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/352636
- This record as JSON: /data/d/352636.json