ODCs

Click node...

3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Dedifferentiated liposarcoma

Autosomal dominant spastic paraplegia type 10


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MDM2	(0.49)	KIF5A

Citations in the biomedical literature:

Dedifferentiated liposarcoma		Autosomal dominant spastic paraplegia type 10
	Synonym(s): - DDLS		Synonym(s): - SPG10

	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: Class of prevalence: unknown 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: - 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: C537482

No signs/symptoms info available.