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
CHD1	gene	CHD1	Expert list;Expert Review Red	Ectodermal Dysplasia		Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Pilarowski-Bjornsson syndrome MIM#617682			Ectodermal dysplasia;HP:0000968	28866611		False	1	50;0;50	0.86	True		ENSG00000153922	ENSG00000153922	HGNC:1915													
ENAM	gene	ENAM	Expert list;Expert Review Red	Ectodermal Dysplasia		Dermatological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	"Amelogenesis imperfecta, type IB, MIM#	104500;Amelogenesis imperfecta, type IC, MIM#	204650"			Ectodermal dysplasia;HP:0000968			False	1	0;0;100	0.86	True		ENSG00000132464	ENSG00000132464	HGNC:3344													
KRT74	gene	KRT74	Expert Review Red;Royal Melbourne Hospital	Ectodermal Dysplasia		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	?Ectodermal dysplasia 7, hair/nail type, 614929			Ectodermal dysplasia;HP:0000968	24714551		False	1	0;50;50	0.86	True		ENSG00000170484	ENSG00000170484	HGNC:28929