ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

3 associated genes
4 signs/symptoms

Dominant hypophosphatemia with nephrolithiasis or osteoporosis

Well-differentiated liposarcoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SLC9A3R1	(0.63)	MDM2

Citations in the biomedical literature:

Dominant hypophosphatemia with nephrolithiasis or osteoporosis		Well-differentiated liposarcoma
	Synonym(s): (no synonyms)		Synonym(s): - ALT - Atypical lipoma - Atypical lipomatous tumor - WDLS

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: adult Type of inheritance: sporadic

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

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
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
(no data available)