ORPHA:324764
Trichorhinophalangeal syndrome
- Type
- Clinical group
- 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 | Trichorhinophalangeal syndrome | |
| fr | Syndrome tricho-rhino-phalangien | |
| de | Tricho-rhino-phalangeales Syndrom | |
| es | Síndrome trico-rino-falángico | |
| it | Sindrome trico-rino-falangea | |
| nl | Trichorinofalangeaal syndroom | |
| pt | Síndrome tricorinofalangeal | |
| pl | Zespół włosowo-nosowo-paliczkowy | |
| cs | Trichorinofalangeální syndrom | |
| uk | Трихоринофаланговий синдром | |
| zh | 毛发-鼻-指(趾)综合征 | |
| tr | Trikorinofalangeal sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017951 | E | validated | |
| MONDO | 17951 | E | validated | |
| UMLS | C0265255 | E | validated | |
| MedDRA | 10051956 | 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 (2):
- ORPHA:93436Acromelic dysplasia
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases - ORPHA:79373Ectodermal dysplasia syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases; rare skin diseases
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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/324764
- This record as JSON: /data/d/324764.json