ORPHA:156215
Oromandibular-limb anomalies syndrome
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Oromandibular-limb anomalies syndrome | |
| fr | Syndrome oro-mandibulaire-anomalies des membres | |
| de | Oromandibuläre Fehlbildung und Extremitätenanomalien | |
| es | Síndrome de anomalía oromandibular y de las extremidades | |
| it | Sindrome da anomalie oromandibolari e degli arti | |
| nl | Oromandibulaire-ledemaatanomalieënsyndroom | |
| pt | Síndrome oromandibular-anomalias dos membros | |
| pl | Zespół wad ustno-żuchwowo-kończynowych | |
| cs | Oromandibulární syndrom s anomáliemi končetin | |
| uk | Синдром рото-нижньощелепних аномалій та аномалій кінцівок | |
| zh | 口下颌-肢体畸形综合征 | |
| tr | Oromandibuler-ekstremite anomalileri sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD25.0 | E | specific | validated |
| MONDO | 0015498 | E | validated | |
| MONDO | 15498 | E | validated | |
| UMLS | C5680663 | 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:156212Hypoglossia/aglossia
rare developmental anomalies during embryogenesis; rare genetic diseases; rare surgical maxillo-facial diseases
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/156215
- This record as JSON: /data/d/156215.json