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Autosomal recessive hypophosphatemic rickets
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Dense deposit disease
1 OMIM reference -
2 associated genes
No signs/symptoms info
Autosomal recessive hypophosphatemic rickets
Dense deposit disease

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

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


Citations in the biomedical literature:


Autosomal recessive hypophosphatemic rickets
DMP1 ENPP1
Dense deposit disease
CFH CFHR1



Autosomal recessive hypophosphatemic rickets
Dense deposit disease

Synonym(s):
- ARHR
Synonym(s):
- Membranoproliferative glomerulonephritis type 2
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D015432
No signs/symptoms info available.