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
COG8	gene	COG8	Expert Review Red;Literature	Hydrocephalus_Ventriculomegaly		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIh 611182			Hydrocephalus;HP:0000238; Ventriculomegaly;HP:0002119	PMID: 30690882		False	1	0;0;100	0.127	True		ENSG00000213380	ENSG00000213380	HGNC:18623													
CWH43	gene	CWH43	Expert Review;Expert Review Red	Hydrocephalus_Ventriculomegaly		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hydrocephalus MONDO:0001150, CWH43-related			Hydrocephalus;HP:0000238; Ventriculomegaly;HP:0002119	33459505;34380733		False	1	0;0;100	0.127	True		ENSG00000109182	ENSG00000109182	HGNC:26133													
FMR1	gene	FMR1	Expert Review Red;Victorian Clinical Genetics Services	Hydrocephalus_Ventriculomegaly		Neurology and neurodevelopmental disorders	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Fragile X syndrome, MIM# 300624			Hydrocephalus;HP:0000238; Ventriculomegaly;HP:0002119			False	1	0;0;100	0.127	True		ENSG00000102081	ENSG00000102081	HGNC:3775													
MYMK	gene	MYMK	Expert Review Red;Victorian Clinical Genetics Services	Hydrocephalus_Ventriculomegaly		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Carey-Fineman-Ziter syndrome;OMIM #254940			Hydrocephalus;HP:0000238; Ventriculomegaly;HP:0002119	28681861		False	1	0;0;100	0.127	True		ENSG00000187616	ENSG00000187616	HGNC:33778													
TOGARAM1	gene	TOGARAM1	Expert Review Red;Literature	Hydrocephalus_Ventriculomegaly		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Cleft of the lip and palate;Microphthalmia;Cerebral dysgenesis;Hydrocephalus			Hydrocephalus;HP:0000238; Ventriculomegaly;HP:0002119	32747439		False	1	0;0;100	0.127	True		ENSG00000198718	ENSG00000198718	HGNC:19959													
ZNF3	gene	ZNF3	Expert Review Red;Literature	Hydrocephalus_Ventriculomegaly		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Hydrocephalus;cleft palate;microphthalmia			Hydrocephalus;HP:0000238; Ventriculomegaly;HP:0002119	32732226		False	1	0;0;100	0.127	True		ENSG00000166526	ENSG00000166526	HGNC:13089