Disease #01677 (MCC1D (3 methylcrotonyl-CoA carboxylase 1 deficiency (MCC1D)), OMIM:210200)

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	Curator: Johan T. den Dunnen

Official abbreviation	MCC1D
Name	3 methylcrotonyl-CoA carboxylase 1 deficiency (MCC1D)
OMIM ID	210200
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MCCC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A