Cytoscape Web
Click node...

Dominant hypophosphatemia with nephrolithiasis or osteoporosis
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
1 associated gene
No signs/symptoms info
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

SLC34A1
(UniProt - OMIM)
 PIK3CA
(UniProt - OMIM)
SLC9A3R1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SLC9A3R1
(0.75)
PIK3CA


Citations in the biomedical literature:


Dominant hypophosphatemia with nephrolithiasis or osteoporosis
SLC34A1 SLC9A3R1
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
PIK3CA



Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.