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
HPGD	gene	HPGD	Expert Review Green;London North GLH;NHS GMS	Autosomal recessive primary hypertrophic osteoarthropathy		Dermatology	BIALLELIC, autosomal or pseudoautosomal	Hypertrophic osteoarthropathy, primary, autosomal recessive 1 OMIM:259100						False	3	100;0;0	1.17	False		ENSG00000164120	ENSG00000164120	HGNC:5154													
SLCO2A1	gene	SLCO2A1	Expert Review Green;London North GLH;NHS GMS	Autosomal recessive primary hypertrophic osteoarthropathy		Dermatology	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Hypertrophic osteoarthropathy, primary, autosomal recessive 2 OMIM:614441;hypertrophic osteoarthropathy, primary, autosomal recessive, 2, MONDO:0013756;Hypertrophic osteoarthropathy, primary, autosomal dominant, OMIM:167100;hypertrophic osteoarthropathy, primary, autosomal dominant, MONDO:0008172				23509104;27134495;33852188;22331663;27134495		False	3	100;0;0	1.17	False		ENSG00000174640	ENSG00000174640	HGNC:10955													
ACVR1	gene	ACVR1	Expert Review Amber;Other	Autosomal recessive primary hypertrophic osteoarthropathy		Dermatology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Fibrodysplasia ossificans progressiva OMIM:135100						False	2	0;0;0	1.17	False		ENSG00000115170	ENSG00000115170	HGNC:171