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
DROSHA	gene	DROSHA	Expert Review Amber;Literature	Hereditary Haemorrhagic Telangiectasia		Vascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Neurodevelopmental disorder, MONDO:0700092;hereditary hemorrhagic telangiectasia MONDO:0019180;idiopathic spontaneous coronary artery dissection MONDO:0007385			Telangiectasia;HP:0001009	39654947;35405010;29339534		False	2	0;100;0	1.6	False		ENSG00000113360	ENSG00000113360	HGNC:17904