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
EGFLAM	gene	EGFLAM	Expert Review Amber;Literature	Congenital Stationary Night Blindness		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Congenital stationary night blindness MONDO:0016293, EGFLAM-related			Congenital stationary night blindness;HP:0007642; Retinal dystrophy;HP:0000556	41343198;18641643		False	2	0;100;0	0.24	False		ENSG00000164318	ENSG00000164318	HGNC:26810