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
	PROM1 Gene (Entity type)	prominin 1
	MAGEA6 Gene (Entity type)	MAGE family member A6
	FABP4 Gene (Entity type)	fatty acid binding protein 4
	CEACAM6 Gene (Entity type)	CEA cell adhesion molecule 6
	TFF1 Gene (Entity type)	trefoil factor 1
	FABP5 Gene (Entity type)	fatty acid binding protein 5
	ISG15 Gene (Entity type)	ISG15 ubiquitin like modifier
	GJA1 Gene (Entity type)	gap junction protein alpha 1
	IFITM1 Gene (Entity type)	interferon induced transmembrane protein 1
	FGFR3 Gene (Entity type)	fibroblast growth factor receptor 3

PROM1

Gene (Entity type)

prominin 1

MAGEA6

Gene (Entity type)

MAGE family member A6

FABP4

Gene (Entity type)

fatty acid binding protein 4

CEACAM6

Gene (Entity type)

CEA cell adhesion molecule 6

TFF1

Gene (Entity type)

trefoil factor 1

FABP5

Gene (Entity type)

fatty acid binding protein 5

ISG15

Gene (Entity type)

ISG15 ubiquitin like modifier

GJA1

Gene (Entity type)

gap junction protein alpha 1

IFITM1

Gene (Entity type)

interferon induced transmembrane protein 1

FGFR3

Gene (Entity type)

fibroblast growth factor receptor 3

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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 2025

This repository is under review for potential modification in compliance with Administration directives.