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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Autosomal recessive hypophosphatemic rickets
Immunoglobulin-mediated membranoproliferative glomerulonephritis

DMP1 CFH
ENPP1 DGKE


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
Immunoglobulin-mediated membranoproliferative glomerulonephritis
CFH DGKE



Autosomal recessive hypophosphatemic rickets
Immunoglobulin-mediated membranoproliferative glomerulonephritis

Synonym(s):
- ARHR

Synonym(s):
- Ig-mediated MPGN
- Ig-mediated membranoproliferative glomerulonephritis
- Immunoglobulin-mediated MPGN

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:
(no data available)

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

No signs/symptoms info available.