ODCs

Click node...

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Intermittent hydrarthrosis

Acrokeratosis verruciformis of Hopf

MEFV	(UniProt - OMIM)		ATP2A2	(UniProt - OMIM)
TNFRSF1A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TNFRSF1A	(0.72)	ATP2A2

Citations in the biomedical literature:

Intermittent hydrarthrosis		Acrokeratosis verruciformis of Hopf

	Classification (Orphanet): - Rare genetic disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): (no data available)		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.