ODCs

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Dominant hypophosphatemia with nephrolithiasis or osteoporosis

Chronic myelomonocytic leukemia

SLC34A1	(UniProt - OMIM)		ETV6	(UniProt - OMIM)
SLC9A3R1	(UniProt - OMIM)		PDGFRB	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SLC9A3R1	(0.97)	PDGFRB

Citations in the biomedical literature:

Dominant hypophosphatemia with nephrolithiasis or osteoporosis		Chronic myelomonocytic leukemia

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare hematologic disease - 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: (no data available)

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references 1 MeSH reference: D015477

No signs/symptoms info available.