ORPHA:1991
Cleft lip with or without cleft palate
Synonyms: Tessier cleft number 1,2
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cleft lip with or without cleft palate | Tessier cleft number 1,2 |
| fr | Fente labiale avec ou sans fente palatine | Fente 1,2 de Tessier |
| de | Lippenspalte mit oder ohne Gaumenspalte | |
| es | Hendidura labial con o sin paladar hendido | Fisura labial con o sin fisura palatina |
| it | Schisi labiale con o senza schisi palatina | |
| nl | Gespleten lip met of zonder gespleten verhemelte | Tessier spleet nummer 1,2 |
| pt | Fenda labial com ou sem fenda palatina | |
| pl | Rozszczep wargi z lub bez rozszczepu podniebienia | Rozszczep Tessiera numer 1,2 |
| cs | Rozštěp rtu s nebo bez rozštěpu patra | Tessier cleft number 1,2 · Rozštěp číslo 1,2 dle Tessiera |
| uk | Розщілина губи з або без розщілини піднебіння | Розщілина Тессьє № 1,2 |
| zh | 唇裂伴或不伴腭裂 | Tessier裂1，2型 |
| tr | Yarık damakla birlikte olan veya olmayan yarık dudak | Tessier yarık sayısı 1,2 |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16034 | E | validated | |
| UMLS | C0810364 | 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 (2):
- ORPHA:155832Rare head and neck malformation
rare developmental anomalies during embryogenesis - ORPHA:68329Rare maxillo-facial surgical disease
rare surgical maxillo-facial diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
3 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Prevalence at birth | 6-9 / 10 000 | — | Worldwide | Class only | Validated | 20507242[PMID] |
| Prevalence at birth | >1 / 1000 | 190.5 / 100 000 | Japan | Value and class | Validated | 22374000[PMID] |
| Prevalence at birth | 6-9 / 10 000 | 77.5 / 100 000 | United States | Value and class | Validated | 22374000[PMID] |
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/1991
- This record as JSON: /data/d/1991.json