raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:414726

Genetic facial cleft

Synonyms: Genetic craniofacial cleft

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enGenetic facial cleftGenetic craniofacial cleft
frFente faciale d'origine génétiqueFente cranio-faciale d'origine génétique
deGesichtsspalte, genetisch bedingteGenetisch bedingte kranio-faziale Spalte
esHendidura facial genéticaHendidura craneofacial genética
itSchisi facciale di origine geneticaSchisi craniofacciale di origine genetica
nlGenetische aangezichtsspleetGenetische craniofaciale splijting
ptFenda facial de origem genética conhecida
plRozszczep twarzo-czaszki uwarunkowany genetycznieRozszczep twarzy uwarunkowany genetycznie
csGeneticky podmíněný rozštěp v obličejiGeneticky podmíněný kraniofaciální rozštěp
ukГенетично обумовлена розщілина обличчяГенетична черепно-лицьова розщелина
zh遗传性面裂遗传性面裂
trGenetik fasiyal yarıkGenetik kraniyofasiyal yarık
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5680068Evalidated

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):

Children (4):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card