ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Radial hemimelia, bilateral

Commissural facial cleft

LMBR1	(UniProt - OMIM)		PTCH2	(UniProt - OMIM)
SHH	(UniProt - OMIM)		SPECC1L	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SHH	(0.52)	PTCH2

Citations in the biomedical literature:

Radial hemimelia, bilateral		Commissural facial cleft
	Synonym(s): - Radial longitidinal meromelia, bilateral		Synonym(s): - Macrostomia

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic 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: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.