ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Pyruvate dehydrogenase E1-alpha deficiency

Immunoglobulin-mediated membranoproliferative glomerulonephritis

PDHA1	(UniProt - OMIM)		CFH	(UniProt - OMIM)
			DGKE	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PDHA1	(0.76)	DGKE

Citations in the biomedical literature:

Pyruvate dehydrogenase E1-alpha deficiency		Immunoglobulin-mediated membranoproliferative glomerulonephritis
	Synonym(s): - PDHAD - Pyruvate decarboxylase deficiency - Pyruvate dehydrogenase complex E1 component subunit alpha deficiency		Synonym(s): - Ig-mediated MPGN - Ig-mediated membranoproliferative glomerulonephritis - Immunoglobulin-mediated MPGN

	Classification (Orphanet): - Inborn errors of metabolism - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: child / adolescent Type of inheritance: x-linked dominant		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.