ODCs

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

PROTEIN INTERACTIONS: 1

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

Alveolar soft-part sarcoma

Intellectual deficit, X-linked, Snyder type

ASPSCR1	(UniProt - OMIM)		SMS	(UniProt - OMIM)
TFE3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TFE3	(0.63)	SMS

Citations in the biomedical literature:

Alveolar soft-part sarcoma		Intellectual deficit, X-linked, Snyder type
	Synonym(s): (no synonyms)		Synonym(s): - Snyder-Robinson syndrome

	Classification (Orphanet): - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic 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: adolescence / young Average age of death: - Type of inheritance: x-linked recessive

	External references: 1 OMIM reference - 1 MeSH reference: D018234		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.