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
	C3 Gene (Entity type)	complement C3
	KYNU Gene (Entity type)	kynureninase
	COL4A5 Gene (Entity type)	collagen type IV alpha 5 chain
	FN1 Gene (Entity type)	fibronectin 1
	GATM Gene (Entity type)	glycine amidinotransferase
	WT1 Gene (Entity type)	WT1 transcription factor
	MAFB Gene (Entity type)	MAF bZIP transcription factor B
	JAG1 Gene (Entity type)	jagged canonical Notch ligand 1
	DDX3Y Gene (Entity type)	DEAD-box helicase 3 Y-linked

TNFSF10

Gene (Entity type)

TNF superfamily member 10

Gene (Entity type)

complement C3

KYNU

Gene (Entity type)

kynureninase

COL4A5

Gene (Entity type)

collagen type IV alpha 5 chain

FN1

Gene (Entity type)

fibronectin 1

GATM

Gene (Entity type)

glycine amidinotransferase

WT1

Gene (Entity type)

WT1 transcription factor

MAFB

Gene (Entity type)

MAF bZIP transcription factor B

JAG1

Gene (Entity type)

jagged canonical Notch ligand 1

DDX3Y

Gene (Entity type)

DEAD-box helicase 3 Y-linked

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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

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