ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 2
PROTEIN INTERACTIONS: 1

3 OMIM references -
2 associated genes
No signs/symptoms info

Axenfeld anomaly

Rieger anomaly

FOXC1	(UniProt - OMIM)		FOXC1	(UniProt - OMIM)
PITX2	(UniProt - OMIM)		PITX2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FOXC1	(0.76)	PITX2

Citations in the biomedical literature:

Axenfeld anomaly		Rieger anomaly

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - 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: 2 OMIM references - No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.