Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
ACADL	gene	ACADL	Expert Review Red;Victorian Clinical Genetics Services	Fatty Acid Oxidation Defects		Metabolic disorders	BIALLELIC, autosomal or pseudoautosomal	Pulmonary surfactant dysfunction			Abnormal circulating fatty acid concentration;HP:0004359; Rhabdomyolysis;HP:0003201; Hypoglycaemia;HP:0001943	24591516;31399326		False	1	0;0;100	1.14	True		ENSG00000115361	ENSG00000115361	HGNC:88													
ACSL5	gene	ACSL5	Expert Review Red;Literature	Fatty Acid Oxidation Defects		Metabolic disorders	BIALLELIC, autosomal or pseudoautosomal	"Diarrhoea 13, MIM# 	620357"			Abnormal circulating fatty acid concentration;HP:0004359; Rhabdomyolysis;HP:0003201; Hypoglycaemia;HP:0001943	PMID: 33191500		False	1	0;0;100	1.14	True		ENSG00000197142	ENSG00000197142	HGNC:16526													
PPARG	gene	PPARG	Expert Review Red;Victorian Clinical Genetics Services	Fatty Acid Oxidation Defects		Metabolic disorders	Unknown				Abnormal circulating fatty acid concentration;HP:0004359; Rhabdomyolysis;HP:0003201; Hypoglycaemia;HP:0001943			False	1	0;0;100	1.14	True		ENSG00000132170	ENSG00000132170	HGNC:9236