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Myxofibrosarcoma

3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Limb-mammary syndrome

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

Myxofibrosarcoma

Limb-mammary syndrome

CREB3L1	(UniProt)		TP63	(UniProt - OMIM)
CREB3L2	(UniProt - OMIM)
FUS	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FUS	(0.76)	TP63

Citations in the biomedical literature:

Myxofibrosarcoma		Limb-mammary syndrome
	Synonym(s): - Fibromyxosarcoma - Myxoid malignant fibrous histiocytoma		Synonym(s): - LMS

	Classification (Orphanet): - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535903

No signs/symptoms info available.