ODCs

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3 associated genes
4 signs/symptoms

PROTEIN INTERACTIONS: 2

1 OMIM reference -
2 associated genes
10 signs/symptoms

Well-differentiated liposarcoma

Epidermolysis bullosa simplex with mottled pigmentation


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MDM2 MDM2	(0.72) (0.63)	KRT14 KRT5

Citations in the biomedical literature:

Well-differentiated liposarcoma		Epidermolysis bullosa simplex with mottled pigmentation
	Synonym(s): - ALT - Atypical lipoma - Atypical lipomatous tumor - WDLS		Synonym(s): - EBS-MP

	Classification (Orphanet): - Rare oncologic disease		Classification (Orphanet): - Rare genetic 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: unknown 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: 1 OMIM reference - 1 MeSH reference: C535959

Well-differentiated liposarcoma		Epidermolysis bullosa simplex with mottled pigmentation
	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		Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Autosomal dominant inheritance - Follicular / erythematous / edematous papules / milium - Irregular / patchy skin hypopigmentation - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Abnormal fingernails - Bruisability - Nails anomalies - Palmoplantar hyperkeratosis / keratoderma - Premature ageing