Disease #03717 (Mitochondrial pyruvate carrier deficiency, OMIM:614741)

Official abbreviation -
Name Mitochondrial pyruvate carrier deficiency
OMIM ID 614741
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MPC1
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Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A