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

Solitary fibrous tumor

Charcot-Marie-Tooth disease type 4E

NAB2	(UniProt - OMIM)		EGR2	(UniProt - OMIM)
STAT6	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NAB2	(0.59)	EGR2

Citations in the biomedical literature:

Solitary fibrous tumor		Charcot-Marie-Tooth disease type 4E
	Synonym(s): (no synonyms)		Synonym(s): - Autosomal recessive congenital hypomyelinating neuropathy - CMT4E

	Classification (Orphanet): - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the nervous system -

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

	External references: 1 OMIM reference - 1 MeSH reference: D006393		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.