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

Early-onset myopathy with fatal cardiomyopathy

3-phosphoglycerate dehydrogenase deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TTN	(0.63)	PHGDH

Citations in the biomedical literature:

Early-onset myopathy with fatal cardiomyopathy		3-phosphoglycerate dehydrogenase deficiency

	Classification (Orphanet): - Rare cardiac disease - 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: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

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

No signs/symptoms info available.