ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Tessier number 4 facial cleft

Commissural facial cleft

SPECC1L	(UniProt - OMIM)		PTCH2	(UniProt - OMIM)
			SPECC1L	(UniProt - OMIM)

Citations in the biomedical literature:

Tessier number 4 facial cleft		Commissural facial cleft
	Synonym(s): (no synonyms)		Synonym(s): - Macrostomia

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.