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
AHCY	gene	AHCY	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	613752			Hydrops fetalis;HP:0001789	30121674;20852937		False	2	0;100;0	0.328	True		ENSG00000101444	ENSG00000101444	HGNC:343													
ALG1	gene	ALG1	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Ik, MIM#608540			Hydrops fetalis;HP:0001789	22966035		False	2	0;100;0	0.328	True		ENSG00000033011	ENSG00000033011	HGNC:18294													
ALPK3	gene	ALPK3	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Cardiomyopathy, familial hypertrophic 27, MIM#	618052"			Hydrops fetalis;HP:0001789	26846950		False	2	0;100;0	0.328	True		ENSG00000136383	ENSG00000136383	HGNC:17574													
BICD2	gene	BICD2	Expert Review Amber;Literature	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Spinal muscular atrophy, lower extremity-predominant 2B, prenatal-onset (MIM#609797)			Hydrops fetalis;HP:0001789	37173812		False	2	0;100;0	0.328	True		ENSG00000185963	ENSG00000185963	HGNC:17208													
CDK10	gene	CDK10	Expert Review Amber;Literature	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Al Kaissi syndrome MIM#617694			Hydrops fetalis;HP:0001789	28886341;34974531		False	2	0;100;0	0.328	True		ENSG00000185324	ENSG00000185324	HGNC:1770													
DYNC2H1	gene	DYNC2H1	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Short-rib thoracic dysplasia 3 with or without polydactyly, MIM#	613091"			Hydrops fetalis;HP:0001789	27925158		False	2	0;100;0	0.328	True		ENSG00000187240	ENSG00000187240	HGNC:2962													
FRAS1	gene	FRAS1	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Fraser syndrome 1, MIM#	219000"			Hydrops fetalis;HP:0001789	27859469		False	2	0;100;0	0.328	True		ENSG00000138759	ENSG00000138759	HGNC:19185													
FZD6	gene	FZD6	Expert Review Amber;Literature	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Hydrops fetalis, MONDO:0015193, FZD6-related			Hydrops fetalis;HP:0001789	33082562;26036949;28425981		False	2	0;100;0	0.328	True		ENSG00000164930	ENSG00000164930	HGNC:4044													
GATA2	gene	GATA2	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Emberger syndrome, MIM#	614038"			Hydrops fetalis;HP:0001789	21892158		False	2	0;100;0	0.328	True		ENSG00000179348	ENSG00000179348	HGNC:4171													
GLDN	gene	GLDN	Expert Review Amber;Literature	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Lethal congenital contracture syndrome 11, MIM# 617194			Hydrops fetalis;HP:0001789	34132406		False	2	0;100;0	0.328	True		ENSG00000186417	ENSG00000186417	HGNC:29514													
IDUA	gene	IDUA	Expert Review Amber;Victorian Clinical Genetics Services	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Hurler syndrome, MPS 1			Hydrops fetalis;HP:0001789	27928775		False	2	0;100;0	0.328	True		ENSG00000127415	ENSG00000127415	HGNC:5391													
KLHL40	gene	KLHL40	Expert Review Amber;Victorian Clinical Genetics Services	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Nemaline myopathy 8, autosomal recessive, MIM# 615348			Hydrops fetalis;HP:0001789	25721947		False	2	0;100;0	0.328	True		ENSG00000157119	ENSG00000157119	HGNC:30372													
MAPK1	gene	MAPK1	Expert Review Amber;Literature	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Noonan syndrome 13 MIM#619087			Hydrops fetalis;HP:0001789	PMID: 32721402		False	2	50;50;0	0.328	True		ENSG00000100030	ENSG00000100030	HGNC:6871													
PDCD2	gene	PDCD2	Expert Review Amber;Literature	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Non-immune hydrops fetalis, MONDO:0009369, PDCD2-related			Hydrops fetalis;HP:0001789	40208938		False	2	0;100;0	0.328	True		ENSG00000071994	ENSG00000071994	HGNC:8762													
PSAT1	gene	PSAT1	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Neu-Laxova syndrome 2, MIM#	616038"			Hydrops fetalis;HP:0001789	30838783;27475004		False	2	100;0;0	0.328	True		ENSG00000135069	ENSG00000135069	HGNC:19129													
SLC26A2	gene	SLC26A2	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Achondrogenesis Ib, MIM#	600972"			Hydrops fetalis;HP:0001789	31880411		False	2	0;100;0	0.328	True		ENSG00000155850	ENSG00000155850	HGNC:10994													
SLC30A5	gene	SLC30A5	Expert Review Amber;Literature	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Cardiomyopathy MONDO:0004994, SLC30A5-related;Perinatal lethal cardiomyopathy			Hydrops fetalis;HP:0001789	33547425;12095919		False	2	0;100;0	0.328	True		ENSG00000145740	ENSG00000145740	HGNC:19089													
TRIP11	gene	TRIP11	Expert list;Expert Review Amber	Hydrops fetalis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Achondrogenesis, type IA, MIM#	200600"			Hydrops fetalis;HP:0001789	30951048;8897040		False	2	0;100;0	0.328	True		ENSG00000100815	ENSG00000100815	HGNC:12305