Cytoscape Web
Click node...

Dominant hypophosphatemia with nephrolithiasis or osteoporosis
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Male infertility with normal virilization due to meiosis defect
4 OMIM references -
3 associated genes
No signs/symptoms info
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Male infertility with normal virilization due to meiosis defect

SLC34A1
(UniProt - OMIM)
 CFTR
(UniProt - OMIM)
SLC9A3R1
(UniProt - OMIM)
 SOHLH1
(UniProt - OMIM)
SYCP3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SLC9A3R1
(0.97)
CFTR


Citations in the biomedical literature:


Dominant hypophosphatemia with nephrolithiasis or osteoporosis
SLC34A1 SLC9A3R1
Male infertility with normal virilization due to meiosis defect
CFTR SOHLH1 SYCP3



Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Male infertility with normal virilization due to meiosis defect

Synonym(s):
(no synonyms)

Synonym(s):
- Azoospermia due to maturation arrest
- Azoospermia due to meiosis defect
- Male infertility with normal virilization due to maturation arrest
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- 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:
Class of prevalence: -
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.