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Dedifferentiated liposarcoma

3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Erythropoietic protoporphyria

2 OMIM references -
2 associated genes
9 signs/symptoms

Dedifferentiated liposarcoma

Erythropoietic protoporphyria

CDK4	(UniProt - OMIM)		ALAS2	(UniProt - OMIM)
HMGA2	(UniProt - OMIM)		FECH	(UniProt - OMIM)
MDM2	(UniProt - OMIM)


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

Citations in the biomedical literature:

Dedifferentiated liposarcoma		Erythropoietic protoporphyria
	Synonym(s): - DDLS		Synonym(s): - EPP - XLDPP

	Classification (Orphanet): - Rare oncologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare renal disease - Rare skin 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 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 2 OMIM references - 1 MeSH reference: D046351

Erythropoietic protoporphyria
	Very frequent - Autosomal dominant inheritance - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Skin photosensitivity - Urticaria Occasional - Biliary / gallbladder stones / lithiasis / cholecystitis - Cirrhosis - Cutaneous edema - Eczema - Microcytic anemia
Dedifferentiated liposarcoma
(no data available)