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
ACD	gene	ACD	Expert Review Amber;Literature	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	pulmonary fibrosis and/or bone marrow failure, telomere-related MONDO:0000148			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	31515401;27807141;25205116		False	2	0;100;0	0.84	True	Other	ENSG00000102977	ENSG00000102977	HGNC:25070