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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
X-linked myopathy with excessive autophagy
Chuvash erythrocytosis

VMA21 VHL


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VMA21
(0.63)
VHL



Citations in the biomedical literature:


X-linked myopathy with excessive autophagy
VMA21
Chuvash erythrocytosis
VHL



X-linked myopathy with excessive autophagy
Chuvash erythrocytosis

Synonym(s):
- Vacuolar myopathy
- XMEA

Synonym(s):
- Chuvash polycythemia
- Von Hippel-Lindau-dependent polycythemia

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.