ODCs

Click node...

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Postaxial polydactyly type A, bilateral

FG syndrome type 1

GLI3	(UniProt - OMIM)		MED12	(UniProt - OMIM)
ZNF141	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GLI3	(0.68)	MED12

Citations in the biomedical literature:

Postaxial polydactyly type A, bilateral		FG syndrome type 1
	Synonym(s): (no synonyms)		Synonym(s): - Opitz-Kaveggia syndrome

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): (no data available)

	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.