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
DCAF15	gene	DCAF15	Expert Review Amber;Other	Hypertrichosis syndromes		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Cornelia de Lange syndrome, MONDO:0016033, DCAF15-related			Hypertrichosis;HP:0000998			False	2	0;100;0	0.46	True		ENSG00000132017	ENSG00000132017	HGNC:25095													
KCNN3	gene	KCNN3	Expert Review Amber;Literature	Hypertrichosis syndromes		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Zimmermann-Laband syndrome 3 MIM#618658			Hypertrichosis;HP:0000998	34907639		False	2	0;100;0	0.46	True		ENSG00000143603	ENSG00000143603	HGNC:6292													
RPS23	gene	RPS23	Expert Review Amber;Victorian Clinical Genetics Services	Hypertrichosis syndromes		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Brachycephaly, trichomegaly, and developmental delay, MIM# 617412			Hypertrichosis;HP:0000998	28257692		False	2	0;100;0	0.46	True		ENSG00000186468	ENSG00000186468	HGNC:10410