OMIM:202110	17,20-lyase deficiency, isolated	CYP17A1,TOY_GENE_OFICIAL1
OMIM:616034	2,4-dienoyl-CoA reductase deficiency	NADK2
OMIM:610006	2-methylbutyrylglycinuria	ACADSB
OMIM:273750	3-M syndrome 1	CUL7
OMIM:612921	3-M syndrome 2	OBSL1
OMIM:614205	3-M syndrome 3	CCDC8
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency	MCCC1
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency	MCCC2
OMIM:231530	3-hydroxyacyl-CoA dehydrogenase deficiency	HADHSC
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency	HIBCH
OMIM:614739	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome	SERAC1
OMIM:250950	3-methylglutaconic aciduria, type I	AUH
OMIM:258501	3-methylglutaconic aciduria, type III	OPA3
