ODCs

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Neonatal inflammatory skin and bowel disease

Intermittent hydrarthrosis

ADAM17	(UniProt - OMIM)		MEFV	(UniProt - OMIM)
			TNFRSF1A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ADAM17	(0.52)	TNFRSF1A

Citations in the biomedical literature:

Neonatal inflammatory skin and bowel disease		Intermittent hydrarthrosis

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

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: autosomal recessive		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.