ORPHA:3263
Syngnathia-cleft palate syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Age of onset
- Antenatal, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syngnathia-cleft palate syndrome | |
| fr | Syndrome de syngnathie-fente palatine | |
| de | Syngnathie - Gaumenspalte | |
| es | Síndrome de singnatia-paladar hendido | |
| it | Singnazia - schisi palatina | |
| nl | Syngnathie - gespleten gehemelte-syndroom | |
| pt | Síndrome de singnatia-fenda palatina | |
| pl | Zrost szczęki i żuchwy - rozszczep podniebienia | |
| cs | Syndrom zahrnující syngnathii a rozštěp patra | |
| uk | Синдром сингнатії-розщілини піднебіння | |
| zh | 连颌畸形-腭裂综合征 | |
| tr | Singnathi-yarık damak sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q18.8 | NTBT | attributed | validated |
| MONDO | 0017981 | E | validated | |
| UMLS | C5680792 | E | validated | |
| GARD | 5091 | 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:139039Orofacial clefting syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases; rare otorhinolaryngological diseases; rare surgical maxillo-facial diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 11 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.
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/3263
- This record as JSON: /data/d/3263.json