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
EPHB4	gene	EPHB4	Expert list	Meiges disease	Lymphatic disorders	Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Autosomal Dominant Lymphatic Related Hydrops Fetalis				PMID: 27400125		False	1	100;0;0	1.20	False		ENSG00000196411	ENSG00000196411	HGNC:3395													
PTPN14	gene	PTPN14	Expert Review Red;Radboud University Medical Center, Nijmegen	Meiges disease	Lymphatic disorders	Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Choanal atresia and lymphedema, 613611				20826270		False	1	100;0;0	1.20	False		ENSG00000152104	ENSG00000152104	HGNC:9647