ODCs

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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

Chuvash erythrocytosis

X-linked myopathy with excessive autophagy


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

Citations in the biomedical literature:

Chuvash erythrocytosis		X-linked myopathy with excessive autophagy
	Synonym(s): - Chuvash polycythemia - Von Hippel-Lindau-dependent polycythemia		Synonym(s): - Vacuolar myopathy - XMEA

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		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		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.