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
ALG1	gene	ALG1	Expert Review Red;Other	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ik, 608540; Hydrops fetalis, nonimmune				9762608;14973778;31420886		False	1	0;50;50	1.95	False		ENSG00000033011	ENSG00000033011	HGNC:18294													
DHCR7	gene	DHCR7	Other	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Smith-Lemli-Opitz syndrome, 270400; SLOS				23137060; 10215064		False	1	100;0;0	1.95	False		ENSG00000172893	ENSG00000172893	HGNC:2860													
DMPK	gene	DMPK	Expert Review Red;Other	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	Other	Myotonic dystrophy 1, OMIM:160900				8140064; 1550167		False	1	100;0;0	1.95	False	Other - please provide details in the comments	ENSG00000104936	ENSG00000104936	HGNC:2933													
EBP	gene	EBP	Literature	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Chondrodysplasia punctata, X-linked dominant, 302960; Conradi Huenermann: Chondrodysplasia punctata				23137060; 6408138		False	1	0;0;0	1.95	False		ENSG00000147155	ENSG00000147155	HGNC:3133													
FH	gene	FH	Literature	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Fumarase deficiency, 606812; Citric-acid cycle defect				23137060; 1557269; 9635293		False	1	0;0;0	1.95	False		ENSG00000091483	ENSG00000091483	HGNC:3700													
GLE1	gene	GLE1	Expert Review Red;Other	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Lethal congenital contracture syndrome 1, 253310;LCCS1;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE;Arthrogryposis, lethal, with anterior horn cell disease, 611890				3993672;3344776;7966188;16892327		False	1	0;100;0	1.95	False		ENSG00000119392	ENSG00000119392	HGNC:4315													
HADHA	gene	HADHA	Literature	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	LCHAD deficiency, 609016				23137060; 11111210		False	1	0;0;0	1.95	False		ENSG00000084754	ENSG00000084754	HGNC:4801													
HBZ	gene	HBZ	Expert Review Red;Other	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	HEMOGLOBIN H HYDROPS FETALIS SYNDROME				9029003		False	1	0;100;0	1.95	False		ENSG00000130656	ENSG00000130656	HGNC:4835													
PSAT1	gene	PSAT1	Expert list;Expert Review Red	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Neu-Laxova syndrome 2, MIM#	616038"				30838783;27475004		False	1	0;100;0	1.95	False		ENSG00000135069	ENSG00000135069	HGNC:19129													
SUMF1	gene	SUMF1	Other	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Multiple sulfatase deficiency,  272200				25305402		False	1	0;0;0	1.95	False		ENSG00000144455	ENSG00000144455	HGNC:20376													
UROS	gene	UROS	Literature	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Porphyria, congenital erythropoietic, 263700; Congenital erythropoietic porphyria; Gunther's disease				23137060; 12533808 		False	1	0;0;0	1.95	False		ENSG00000188690	ENSG00000188690	HGNC:12592													
DMPK_CTG	str	DMPK	NHS GMS;Expert Review Red;Expert list	Fetal hydrops	Fetal disorders	Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Myotonic dystrophy 1, OMIM:160900						False	1	100;0;0	1.95	False		ENSG00000104936	ENSG00000104936	HGNC:2933	19	46273463	46273522	45770205	45770264	CTG	35	50