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FG syndrome type 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Polysyndactyly, bilateral
1 associated gene
No signs/symptoms info
FG syndrome type 1
Polysyndactyly, bilateral

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

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


Citations in the biomedical literature:


FG syndrome type 1
MED12
Polysyndactyly, bilateral
GLI3



FG syndrome type 1
Polysyndactyly, bilateral

Synonym(s):
- Opitz-Kaveggia syndrome
Synonym(s):
- Preaxial polydactyly type 4, bilateral
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic 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:
No OMIM references
No MeSH references
No signs/symptoms info available.