Alopecia (Phenotype)

Synonyms:HP:0002238, HP:0008068, Hair loss

Id:HP:0001596

Description:A noncongenital process of hair loss, which may progress to partial or complete baldness.

Results found

Linked to

	Label	Description
	LTF Gene (Entity type)	lactotransferrin
	GNAS Gene (Entity type)	GNAS complex locus
	SPP1 Gene (Entity type)	secreted phosphoprotein 1
	KRT14 Gene (Entity type)	keratin 14
	FABP4 Gene (Entity type)	fatty acid binding protein 4
	MGP Gene (Entity type)	matrix Gla protein
	KRT5 Gene (Entity type)	keratin 5
	GJA1 Gene (Entity type)	gap junction protein alpha 1
	SCGB2A1 Gene (Entity type)	secretoglobin family 2A member 1
	STUB1 Gene (Entity type)	STIP1 homology and U-box containing protein 1

LTF

Gene (Entity type)

lactotransferrin

GNAS

Gene (Entity type)

GNAS complex locus

SPP1

Gene (Entity type)

secreted phosphoprotein 1

KRT14

Gene (Entity type)

keratin 14

FABP4

Gene (Entity type)

fatty acid binding protein 4

MGP

Gene (Entity type)

matrix Gla protein

KRT5

Gene (Entity type)

keratin 5

GJA1

Gene (Entity type)

gap junction protein alpha 1

SCGB2A1

Gene (Entity type)

secretoglobin family 2A member 1

STUB1

Gene (Entity type)

STIP1 homology and U-box containing protein 1

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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.