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X-linked myopathy with excessive autophagy
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Chuvash erythrocytosis
Von Hippel-Lindau disease
Hirschsprung disease
Neuralgic amyotrophy
Succinyl-CoA:3-ketoacid CoA transferase deficiency
- Vacuolar myopathy

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
VMA21 Q3ZAQ7300913
No signs/symptoms info available.