Sensorineural hearing impairment (Phenotype)

Synonyms:HP:0000374, HP:0001753, HP:0001916, HP:0008538, HP:0008553, HP:0008565, HP:0008576, HP:0008611, HP:0008613, HP:0008614, Hearing loss, sensorineural, Sensorineural deafness, Sensorineural hearing loss

Id:HP:0000407

Description:A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.

Results found

Linked to

	Label	Description
	LTF Gene (Entity type)	lactotransferrin
	GNAS Gene (Entity type)	GNAS complex locus
	ID1 Gene (Entity type)	inhibitor of DNA binding 1
	PROM1 Gene (Entity type)	prominin 1
	DKK1 Gene (Entity type)	dickkopf Wnt signaling pathway inhibitor 1
	MAGEA6 Gene (Entity type)	MAGE family member A6
	GJA1 Gene (Entity type)	gap junction protein alpha 1
	TFF1 Gene (Entity type)	trefoil factor 1
	ISG15 Gene (Entity type)	ISG15 ubiquitin like modifier
	HPGD Gene (Entity type)	15-hydroxyprostaglandin dehydrogenase

LTF

Gene (Entity type)

lactotransferrin

GNAS

Gene (Entity type)

GNAS complex locus

ID1

Gene (Entity type)

inhibitor of DNA binding 1

PROM1

Gene (Entity type)

prominin 1

DKK1

Gene (Entity type)

dickkopf Wnt signaling pathway inhibitor 1

MAGEA6

Gene (Entity type)

MAGE family member A6

GJA1

Gene (Entity type)

gap junction protein alpha 1

TFF1

Gene (Entity type)

trefoil factor 1

ISG15

Gene (Entity type)

ISG15 ubiquitin like modifier

HPGD

Gene (Entity type)

15-hydroxyprostaglandin dehydrogenase

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Community

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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