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Dominant hypophosphatemia with nephrolithiasis or osteoporosis
2 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Primary Fanconi syndrome
3 OMIM references -
2 associated genes
No signs/symptoms info
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Primary Fanconi syndrome

SLC34A1
(UniProt - OMIM)
 EHHADH
(UniProt - OMIM)
SLC9A3R1
(UniProt - OMIM)
 SLC34A1
(UniProt - OMIM)

COMMON
GENES 		SLC34A1
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SLC9A3R1
(0.59)
SLC34A1


Citations in the biomedical literature:


Dominant hypophosphatemia with nephrolithiasis or osteoporosis
SLC34A1 SLC9A3R1
Primary Fanconi syndrome
EHHADH



Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Primary Fanconi syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Primary Fanconi renotubular syndrome
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.