KFPT:PT-J20GACQ1 CUI (KFPT)

Description: A kfpt in the knowledge graph

Analyze

CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View KFPT:PT-J20GACQ1 CUI's neighborhood in the knowledge graph.

Submit

Knowledge Graph Assertions

Source	Relation	Target
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Retinal vascular tortuosity Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Branchioma Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Tetralogy of Fallot Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Preauricular dimple Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Microcephaly (physical finding) Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormality of abdominal situs Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital scar Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal aortic morphology Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital blindness Disease or Phenotype (Entity type)
KFPT:PT-J20GACQ1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal coronary artery morphology Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Retinal vascular tortuosity
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Branchioma
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Tetralogy of Fallot
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Preauricular dimple
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Microcephaly (physical finding)
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormality of abdominal situs
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital scar
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal aortic morphology
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital blindness
Disease or Phenotype (Entity type)

KFPT:PT-J20GACQ1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal coronary artery morphology
Disease or Phenotype (Entity type)

DISPLAY PER PAGE

CFDE Workbench

Consortium

Community

Resources

@CFDE Workbench 2025

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.