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Dedifferentiated liposarcoma

3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Xeroderma pigmentosum variant

1 OMIM reference -
1 associated gene
10 signs/symptoms

Dedifferentiated liposarcoma

Xeroderma pigmentosum variant

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


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

Citations in the biomedical literature:

Dedifferentiated liposarcoma		Xeroderma pigmentosum variant
	Synonym(s): - DDLS		Synonym(s): - XPV

	Classification (Orphanet): - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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: adolescence / young Average age of death: - Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536766

Xeroderma pigmentosum variant
	Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Autosomal recessive inheritance - Excessive freckling - Skin photosensitivity - Telangiectasic erythema / poikiloderma - Warts / papillomas Frequent - Dry / squaly skin / exfoliation - Skin hypoplasia / aplasia / atrophy - Skin / cutaneous neoplasm / tumor / carcinoma / cancer (excluding melanoma) - Telangiectasiae of the skin
Dedifferentiated liposarcoma
(no data available)