ODCs

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1 OMIM reference -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Extraskeletal myxoid chondrosarcoma

Autosomal recessive optic atrophy, OPA7 type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EWSR1	(0.49)	TMEM126A

Citations in the biomedical literature:

Extraskeletal myxoid chondrosarcoma		Autosomal recessive optic atrophy, OPA7 type

	Classification (Orphanet): - Rare oncologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare genetic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the eye and adnexa -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: adult Type of inheritance: sporadic		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.