ODCs

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2 OMIM references -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Atypical hemolytic uremic syndrome with H factor anomaly

Autosomal recessive hypophosphatemic rickets

CFH	(UniProt - OMIM)		DMP1	(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:

Atypical hemolytic uremic syndrome with H factor anomaly		Autosomal recessive hypophosphatemic rickets
	Synonym(s): - Atypical HUS with H factor anomaly - D-HUS with H factor anomaly - Hemolytic-uremic syndrome without diarrhea with H factor anomaly - aHUS with H factor anomaly		Synonym(s): - ARHR

	Classification (Orphanet): - Rare genetic disease - Rare hematologic 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): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.