ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Intermittent hydrarthrosis

Progressive sensorineural hearing loss - hypertrophic cardiomyopathy

MEFV	(UniProt - OMIM)		MYO6	(UniProt - OMIM)
TNFRSF1A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TNFRSF1A	(0.72)	MYO6

Citations in the biomedical literature:

Intermittent hydrarthrosis		Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
	Synonym(s): (no synonyms)		Synonym(s): - Progressive neurosensory deafness - hypertrophic cardiomyopathy - Progressive neurosensory hearing loss - hypertrophic cardiomyopathy - Progressive sensorineural deafness - hypertrophic cardiomyopathy

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.