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
ACADS	gene	ACADS	Expert Review Amber;Victorian Clinical Genetics Services	Fatty Acid Oxidation Defects		Metabolic disorders	BIALLELIC, autosomal or pseudoautosomal	Acyl-CoA dehydrogenase, short-chain, deficiency of, MIM# 201470;MONDO:0008722			Abnormal circulating fatty acid concentration;HP:0004359; Rhabdomyolysis;HP:0003201; Hypoglycaemia;HP:0001943			False	2	0;100;0	1.14	True		ENSG00000122971	ENSG00000122971	HGNC:90