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

Brody myopathy

Phosphoenolpyruvate carboxykinase 1 deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ATP2A1	(0.63)	PCK1

Citations in the biomedical literature:

Brody myopathy		Phosphoenolpyruvate carboxykinase 1 deficiency
	Synonym(s): (no synonyms)		Synonym(s): - PEPCK1 deficiency

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C536607		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.