ODCs

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Oculootodental syndrome

Intermittent hydrarthrosis

FADD	(UniProt - OMIM)		MEFV	(UniProt - OMIM)
FGF3	(UniProt - OMIM)		TNFRSF1A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FADD	(0.95)	TNFRSF1A

Citations in the biomedical literature:

Oculootodental syndrome		Intermittent hydrarthrosis
	Synonym(s): - OOD		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare genetic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): (no data available)

	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.