ORPHA:664372
Soft and hard cleft palate
Synonyms: Combined form of soft and hard cleft palate · Isolated cleft of the soft and hard palate
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Multigenic/multifactorial
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Soft and hard cleft palate | Combined form of soft and hard cleft palate · Isolated cleft of the soft and hard palate |
| fr | Fente vélo-palatine | |
| de | Hart- und Weichgaumenspalte | Isolierte Spaltbildung des weichen und harten Gaumens · Kombinierte Form der weichen und harten Gaumenspalte |
| es | Hendidura del paladar blando y duro | Forma combinada de paladar hendido blando y duro · Hendidura aislada del paladar blando y duro |
| it | Schisi del palato molle e duro | Forma combinata di schisi del palato molle e duro · Schisi isolata del palato molle e duro |
| nl | Gespleten zacht en hard gehemelte | Schisis van palatum molle en palatum durum · Gecombineerde vorm van gespleten zacht en hard gehemelte · Geïsoleerde spleet van zacht en hard gehemelte |
| pt | Fenda palato mole e duro | Fenda isolada do palato mole e duro · Forma combinada de fenda do palato mole e duro |
| pl | Rozszczep podniebienia miękkiego i twardego | = en |
| cs | Rozštěp měkkého a tvrdého patra | = en |
| uk | Розщілина мякого та твердого піднебіння | Комбінована форма розщілини мякого та твердого піднебіння · Ізольована розщілина мякого та твердого піднебіння |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q35.5 | E | specific | validated |
| MONDO | 0971092 | E | validated | |
| MONDO | 971092 | 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:2014Cleft palate
rare developmental anomalies during embryogenesis; rare surgical maxillo-facial diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
4 annotations · validated 2024-07-09| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0000689 | Dental malocclusion | |
| HP:0001611 | Hypernasal speech | |
| HP:0000327 | Hypoplasia of the maxilla | |
| Occasional (29-5%) | ||
| HP:0000347 | Micrognathia | |
Annotation source: 37436176[PMID]_33976983[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/664372
- This record as JSON: /data/d/664372.json