Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
GALLOWAY MOWAT SYNDROME	C0795949 MESH:C537548	GON7	Unknown	—	Disgenet
		LAGE3	Unknown	28805828	CTD Disgenet
		NUP107	Unknown	—	Disgenet
		NUP133	Unknown	—	Disgenet
		OSGEP	Unknown	28805828	CTD Disgenet
		TP53RK	Unknown	28805828	CTD Disgenet
		TPRKB	Unknown	28805828	CTD Disgenet
		WDR4	Unknown	—	Disgenet
		WDR73	Unknown	25466283	CTD Disgenet
		YRDC	Unknown	—	Disgenet
		ZNF592	Unknown	—	Disgenet
GALLOWAY-MOWAT SYNDROME	2065 MONDO:0009627	GON7	Causal	31481669	Orphanet
		OSGEP	Causal	28805828	GWAS catalog Orphanet
		WDR4	Causal	30079490	GWAS catalog Orphanet
		LAGE3	Unknown	28805828	CTD Orphanet
		NUP107	Unknown	28280135	Orphanet
		NUP133	Unknown	30427554	CTD Orphanet
		TP53RK	Unknown	28805828	GWAS catalog Orphanet
		TPRKB	Unknown	28805828	GWAS catalog Orphanet
		WDR73	Unknown	25466283	GWAS catalog Orphanet
		YRDC	Unknown	31481669	Orphanet
GALLOWAY-MOWAT SYNDROME 1	251300 C4551772 MONDO:0033005	WDR73	Causal	234962 245506 249012 251300 25466283 25873735 26123727 27001912	ClinGen ClinVar Disgenet HPO
GALLOWAY-MOWAT SYNDROME 1	251300 C4551772 MONDO:0033005	ZNF592	Unknown	—	Disgenet
GALLOWAY-MOWAT SYNDROME 10	619609 C5562020 MONDO:0030476	YRDC	Causal	31481669	ClinVar Disgenet GWAS catalog HPO
GALLOWAY-MOWAT SYNDROME 10	619609 C5562020 MONDO:0030476	C1ORF122	Unknown	—	Disgenet
GALLOWAY-MOWAT SYNDROME 2, X-LINKED	301006 C4538784 MONDO:0033006	LAGE3	Causal	22805828 28805828	ClinVar Disgenet HPO
GALLOWAY-MOWAT SYNDROME 3	617729 C4540266 MONDO:0033007	OSGEP	Causal	28272532 28805828 30558655 30975089	CTD ClinVar Disgenet HPO
GALLOWAY-MOWAT SYNDROME 4	617730 C4540270 MONDO:0033008	TP53RK	Causal	28805828 30053862	ClinVar Disgenet GWAS catalog HPO
GALLOWAY-MOWAT SYNDROME 5	617731 C4540274 MONDO:0033009	TPRKB	Causal	28805828 30053862	ClinVar Disgenet HPO Orphanet
GALLOWAY-MOWAT SYNDROME 6	618347 C5193043 MONDO:0032691	WDR4	Causal	30079490	ClinVar Disgenet HPO
GALLOWAY-MOWAT SYNDROME 7	618348 C5193044 MONDO:0032692	NUP107	Causal	26411495 28280135 30179222	CTD ClinVar Disgenet HPO
GALLOWAY-MOWAT SYNDROME 8	618349 C5193045 MONDO:0032693	NUP133	Causal	30427554	ClinVar Disgenet GWAS catalog HPO
GALLOWAY-MOWAT SYNDROME 9	619603 C5562016 MONDO:0030471	GON7	Causal	—	ClinVar Disgenet HPO

Galloway-mowat syndrome