Glaucoma (Phenotype)

Id:HP:0000501

Description:Glaucoma refers loss of retinal ganglion cells in a characteristic pattern of optic neuropathy usually associated with increased intraocular pressure.

Results found

Linked to

	Label	Description
	FABP4 Gene (Entity type)	fatty acid binding protein 4
	PROM1 Gene (Entity type)	prominin 1
	CYP1B1 Gene (Entity type)	cytochrome P450 family 1 subfamily B member 1
	MAGEA6 Gene (Entity type)	MAGE family member A6
	CEACAM6 Gene (Entity type)	CEA cell adhesion molecule 6
	GJA1 Gene (Entity type)	gap junction protein alpha 1
	TFF1 Gene (Entity type)	trefoil factor 1
	ISG15 Gene (Entity type)	ISG15 ubiquitin like modifier
	FGFR3 Gene (Entity type)	fibroblast growth factor receptor 3
	IFITM1 Gene (Entity type)	interferon induced transmembrane protein 1

FABP4

Gene (Entity type)

fatty acid binding protein 4

PROM1

Gene (Entity type)

prominin 1

CYP1B1

Gene (Entity type)

cytochrome P450 family 1 subfamily B member 1

MAGEA6

Gene (Entity type)

MAGE family member A6

CEACAM6

Gene (Entity type)

CEA cell adhesion molecule 6

GJA1

Gene (Entity type)

gap junction protein alpha 1

TFF1

Gene (Entity type)

trefoil factor 1

ISG15

Gene (Entity type)

ISG15 ubiquitin like modifier

FGFR3

Gene (Entity type)

fibroblast growth factor receptor 3

IFITM1

Gene (Entity type)

interferon induced transmembrane protein 1

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@CFDE Workbench 2026

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

Consortium

Community

Resources

CFDE Workbench

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

@CFDE Workbench 2026