ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

4 OMIM references -
3 associated genes
No signs/symptoms info

Intermittent hydrarthrosis

Congenital glaucoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TNFRSF1A	(0.63)	MYOC

Citations in the biomedical literature:

Intermittent hydrarthrosis		Congenital glaucoma

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.