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

Intermittent hydrarthrosis

Oculootodental syndrome

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


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

Citations in the biomedical literature:

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

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

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

	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.