Chronic kidney disease (Phenotype)

Synonyms:HP:0000106, HP:0001918, HP:0008671, Chronic kidney disease, CKD

Id:HP:0012622

Description:Functional anomaly of the kidney persisting for at least three months.

Results found

Linked to

	Label	Description
	TNFSF10 Gene (Entity type)	TNF superfamily member 10
	COL4A5 Gene (Entity type)	collagen type IV alpha 5 chain
	MAFB Gene (Entity type)	MAF bZIP transcription factor B
	C3 Gene (Entity type)	complement C3
	WT1 Gene (Entity type)	WT1 transcription factor
	NUP85 Gene (Entity type)	nucleoporin 85
	SU002653 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001645 project
	DDX3Y Gene (Entity type)	DEAD-box helicase 3 Y-linked
	JAG1 Gene (Entity type)	jagged canonical Notch ligand 1
	FN1 Gene (Entity type)	fibronectin 1

TNFSF10

Gene (Entity type)

TNF superfamily member 10

COL4A5

Gene (Entity type)

collagen type IV alpha 5 chain

MAFB

Gene (Entity type)

MAF bZIP transcription factor B

C3

Gene (Entity type)

complement C3

WT1

Gene (Entity type)

WT1 transcription factor

NUP85

Gene (Entity type)

nucleoporin 85

SU002653

Subject (Entity type)

A subject from Metabolomics produced as part of the PR001645 project

DDX3Y

Gene (Entity type)

DEAD-box helicase 3 Y-linked

JAG1

Gene (Entity type)

jagged canonical Notch ligand 1

FN1

Gene (Entity type)

fibronectin 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