ORPHA:444316
Idiopathic phalangeal acro-osteolysis
Synonyms: Idiopathic phalangeal acroosteolysis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare bone disease characterized by bone resorption affecting the distal phalanx, most commonly the terminal tuft, in the absence of a known cause. Patients present with shortening of the affected fingers or toes, associated with nail abnormalities (dystrophic or hypertrophic nails) and skin changes (such as ulceration or pigment anomalies).
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic phalangeal acro-osteolysis | Idiopathic phalangeal acroosteolysis |
| fr | Acro-ostéolyse phalangienne idiopathique | Acroostéolyse phalangienne idiopathique |
| de | Akroosteolyse, idiopathische phalangeale | |
| es | Acro-osteólisis falángica idiopática | Acroosteólisis falángica idiopática |
| it | Acro-osteolisi idiopatica delle falangi | Acroosteolisi falangea idiopatica |
| nl | Idiopathische falangeale acro-osteolyse | |
| pt | Acrosteólise idiopática das falanges | |
| pl | Idiopatyczna akroosteoliza paliczków | = en |
| cs | Idiopatická falangeální akroosteolýza | Idiopatická falangeální akro-osteolýza |
| uk | Ідіопатичний фаланговий акроостеоліз | Ідіопатичний фаланговий акроостеоліз |
| zh | 特发性指骨肢端溶解 | 特发性指骨肢端溶解 |
| tr | İdiyopatik falangeal akro-osteoliz | İdiyopatik falanjiyal akroosteoliz |
Definition in:
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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 | 0018635 | E | validated | |
| UMLS | C5680064 | E | validated |
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):
- ORPHA:399158Osteonecrosis
rare systemic and rheumatological diseases; rare bone diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/444316
- This record as JSON: /data/d/444316.json