ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Chronic myelomonocytic leukemia

Dominant hypophosphatemia with nephrolithiasis or osteoporosis

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


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

Citations in the biomedical literature:

Chronic myelomonocytic leukemia		Dominant hypophosphatemia with nephrolithiasis or osteoporosis

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.