ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Dense deposit disease

Autosomal recessive hypophosphatemic rickets

CFH	(UniProt - OMIM)		DMP1	(UniProt - OMIM)
CFHR1	(UniProt - OMIM)		ENPP1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CFH	(0.52)	DMP1

Citations in the biomedical literature:

Dense deposit disease		Autosomal recessive hypophosphatemic rickets
	Synonym(s): - Membranoproliferative glomerulonephritis type 2		Synonym(s): - ARHR

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: D015432		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.