ORPHA:93449
Primary osteolysis
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Primary osteolysis | |
| fr | Ostéolyse primaire | |
| de | Osteolyse, primäre | |
| es | Osteólisis primaria | |
| it | Osteolisi primitiva | |
| nl | Primaire osteolyse | |
| pt | Osteólise rara | |
| pl | Rzadki rodzaj osteolizy | |
| cs | Primární osteolýzy | |
| uk | Первинний остеоліз | |
| zh | 原发性骨质溶解 | |
| tr | Primer osteoliz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019707 | E | validated | |
| UMLS | C5559806 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:364526Primary bone dysplasia
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases
Children (13):
- ORPHA:2776Autosomal recessive distal osteolysis syndrome
- ORPHA:1952Epiphyseal stippling-osteoclastic hyperplasia syndrome
- ORPHA:85195Familial expansile osteolysis
- ORPHA:955Hajdu-Cheney syndrome
- ORPHA:740Hutchinson-Gilford progeria syndrome
- ORPHA:498474Hyaline fibromatosis syndrome
- ORPHA:2457Mandibuloacral dysplasia
- ORPHA:647667Mandibuloacral dysplasia associated to MTX2
- ORPHA:2774Multicentric carpo-tarsal osteolysis with or without nephropathy
- ORPHA:371428Multicentric osteolysis-nodulosis-arthropathy spectrum
- ORPHA:280576Nestor-Guillermo progeria syndrome
- ORPHA:352636Phalangeal microgeodic syndrome
- ORPHA:50809Talo-patello-scaphoid osteolysis
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/93449
- This record as JSON: /data/d/93449.json