Disease #01678 (MCC2D (3-methylcrotonyl CoA carboxylase 2 deficiency (MCC2D)), OMIM:210210)

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Official abbreviation	MCC2D
Name	3-methylcrotonyl CoA carboxylase 2 deficiency (MCC2D)
OMIM ID	210210
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MCCC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A