Disease #00046

Official abbreviation	261650
Name	PEPCK deficiency, mitochondrial, 261650 (1)
OMIM ID	261650
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 2 genes	, PCK2
Associated tissues	-
Disease features	-
Remarks	-