Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	References	Source
CONGENITAL CATARACT	C0009691	AGK	—	Disgenet
		BCOR	—	Disgenet
		BFSP1	—	Disgenet
		BFSP2	—	Disgenet
		C14ORF39	—	Disgenet
		CHMP4B	—	Disgenet
		COL4A1	—	Disgenet
		CRYAA	—	Disgenet
		CRYAB	—	Disgenet
		CRYBA1	—	Disgenet
		CRYBA2	—	Disgenet
		CRYBA4	—	Disgenet
		CRYBB1	—	Disgenet
		CRYBB2	—	Disgenet
		CRYBB3	—	Disgenet
		CRYGA	—	Disgenet
		CRYGB	—	Disgenet
		CRYGC	—	Disgenet
		CRYGD	—	Disgenet
		CRYGS	—	Disgenet
		CYP51A1	—	Disgenet
		EPHA2	—	Disgenet
		ERO1B	—	Disgenet
		FBN1	—	Disgenet
		FOXE3	—	Disgenet
CATARACT, CORTICAL, JUVENILE-ONSET	MESH:C566955	BFSP1	—	CTD
CATARACT, PULVERULENT	C1833118	BFSP2	—	Disgenet
		CRYBB1	—	Disgenet
		CRYBB2	—	Disgenet
		CRYGC	—	Disgenet
		CRYGD	—	Disgenet
CATARACT, AUTOSOMAL DOMINANT, MULTIPLE TYPES 1	MESH:C566909	BFSP2	—	CTD
CATARACT, CENTRAL SACCULAR, WITH SUTURAL OPACITIES	C1854021	BFSP2	—	Disgenet
		CRYBA1	—	Disgenet
		CRYBB2	—	Disgenet
		CRYGS	—	Disgenet
CATARACT, POSTERIOR POLAR, 3	C1854311 MESH:C535343	CHMP4B	—	CTD Disgenet
CATARACT, ANTERIOR POLAR	C1855179	CRYAA	—	Disgenet
		CRYBA2	—	Disgenet
		CRYBB3	—	Disgenet
		CRYGB	—	Disgenet
CATARACT, AUTOSOMAL DOMINANT	C1858679 MESH:C565815	CRYAA	—	CTD Disgenet
CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES	C1833229 MESH:C563435	CRYBA1	—	CTD Disgenet
CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 3	MESH:C566923	CRYBB1	—	CTD
CATARACT, CONGENITAL, CERULEAN TYPE 1	C0344523	CRYBB2	—	Disgenet
CATARACT, CONGENITAL, CERULEAN TYPE 1	C0344523	CRYGD	—	Disgenet
CATARACT, CONGENITAL, CERULEAN TYPE, 2	C1832175	CRYBB2	—	Disgenet
CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 2	C1857853 MESH:C565725	CRYBB3	—	CTD Disgenet
CATARACT, COPPOCK-LIKE	C1852438 MESH:C565133	CRYGC	—	CTD Disgenet
CATARACT, POSTERIOR POLAR, 1	C1861825	EPHA2	—	Disgenet

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Congenital cataract