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Well-differentiated liposarcoma

3 associated genes
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Medium chain acyl-CoA dehydrogenase deficiency

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

Well-differentiated liposarcoma

Medium chain acyl-CoA dehydrogenase deficiency

CDK4	(UniProt - OMIM)		ACADM	(UniProt - OMIM)
HMGA2	(UniProt - OMIM)
MDM2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MDM2	(0.63)	ACADM

Citations in the biomedical literature:

Well-differentiated liposarcoma		Medium chain acyl-CoA dehydrogenase deficiency
	Synonym(s): - ALT - Atypical lipoma - Atypical lipomatous tumor - WDLS		Synonym(s): - ACADM deficiency - Carnitine deficiency secondary to medium-chain acyl-CoA dehydrogenase deficiency - MCAD deficiency - MCADD

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

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: adult Type of inheritance: sporadic		Epidemiological data: Class of prevalence: 1-9 / 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: 1 OMIM reference - 1 MeSH reference: C536038

Well-differentiated liposarcoma
	Very frequent - Soft tissue sarcoma / cancer / tumor / liposarcoma / myosarcoma - Subcutaneous nodules / lipomas / tumefaction / swelling Occasional - Functional anomalies of the kidney and the urinary tract - Intestinal transit disorder
Medium chain acyl-CoA dehydrogenase deficiency
(no data available)