ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Chronic berylliosis

Familial vesicoureteral reflux

HLA-DPB1	(UniProt - OMIM)		ROBO2	(UniProt - OMIM)
			SOX17	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HLA-DPB1	(0.63)	ROBO2

Citations in the biomedical literature:

Chronic berylliosis		Familial vesicoureteral reflux
	Synonym(s): - Berylliosis - Beryllium granulomatosis - Beryllium pneumonosis - Chronic beryllium disease - Chronic beryllium lung disease		Synonym(s): - Familial VUR

	Classification (Orphanet): - Rare respiratory disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital disease

	Classification (ICD10): - Diseases of the respiratory system -		Classification (ICD10): - Diseases of the genitourinary system -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: D001607		External references: 7 OMIM references - No MeSH references

No signs/symptoms info available.