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phosphoenolpyruvate carboxykinase deficiency, mitochondrial

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Uniprot Description Metabolic disorder resulting from impaired gluconeogenesis. It is a rare disease with less than 10 cases reported in the literature. Clinical characteristics include hypotonia, hepatomegaly, failure to thrive, lactic acidosis and hypoglycemia. Autopsy reveals fatty infiltration of both the liver and kidneys. The disorder is transmitted as an autosomal recessive trait.
Mondo Term and Equivalent IDs
MONDO:0009864:  phosphoenolpyruvate carboxykinase deficiency, mitochondrial
GARD:0004279: 
MESH:C564890: 
UMLS:C1849821: