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KFPT:PT-NRH3D7MX CUI (KFPT)

Description: A kfpt in the knowledge graph

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CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View KFPT:PT-NRH3D7MX CUI's neighborhood in the knowledge graph.

Knowledge Graph Assertions

	Source	Relation	Target	Evidence
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital blindness Disease or Phenotype (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Microcephaly (physical finding) Disease or Phenotype (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Tetralogy of Fallot Disease or Phenotype (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal aortic morphology Disease or Phenotype (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Conotruncal defect Disease or Phenotype (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Retinal vascular tortuosity Disease or Phenotype (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Limited eye motility from Duane anomaly Disease or Phenotype (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Belongs to cohort Knowledge Graph Relation (Entity type)	Kids First: Congenital Heart Defects KFCOHORT (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital scar Disease or Phenotype (Entity type)
	KFPT:PT-NRH3D7MX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal coronary artery morphology Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital blindness
Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Microcephaly (physical finding)
Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Tetralogy of Fallot
Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal aortic morphology
Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Conotruncal defect
Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Retinal vascular tortuosity
Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Limited eye motility from Duane anomaly
Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Belongs to cohort
Knowledge Graph Relation (Entity type)
Kids First: Congenital Heart Defects
KFCOHORT (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital scar
Disease or Phenotype (Entity type)

KFPT:PT-NRH3D7MX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal coronary artery morphology
Disease or Phenotype (Entity type)

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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.

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Community

Resources

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