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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Nephrogenic diabetes insipidus
Adult-onset distal myopathy due to VCP mutation

AQP2 VCP
AVPR2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
AVPR2
(0.63)
VCP



Citations in the biomedical literature:


Nephrogenic diabetes insipidus
AQP2 AVPR2
Adult-onset distal myopathy due to VCP mutation
VCP



Nephrogenic diabetes insipidus
Adult-onset distal myopathy due to VCP mutation

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
1 MeSH reference: D018500
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.