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

Spinocerebellar ataxia type 28

MEFV	(UniProt - OMIM)		AFG3L2	(UniProt - OMIM)
TNFRSF1A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TNFRSF1A	(0.72)	AFG3L2

Citations in the biomedical literature:

Intermittent hydrarthrosis		Spinocerebellar ataxia type 28
	Synonym(s): (no synonyms)		Synonym(s): - SCA28

	Classification (Orphanet): - Rare genetic disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537205

No signs/symptoms info available.