|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Pyruvate dehydrogenase phosphatase deficiency is a very rare subtype of pyruvate dehydrogenase deficiency (PDHD, see this term) characterized by lactic acidemia in the neonatal period. (Orphanet Rare Disease Ontology, Orphanet_79246)|
|Downloads & Tools|
1 genes associated with the pyruvate dehydrogenase phosphatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
|PDP1||pyruvate dehyrogenase phosphatase catalytic subunit 1|