KFPT:PT-PX1N9AWZ 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-PX1N9AWZ CUI's neighborhood in the knowledge graph.

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Knowledge Graph Assertions

Source	Relation	Target
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Port-Wine Stain Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Left Isomerism Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Holoprosencephaly Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal coronary artery morphology Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Decreased projection of lower jaw Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal aortic morphology Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Pyloric Stenosis, Hypertrophic Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hand polydactyly Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital scar Disease or Phenotype (Entity type)
KFPT:PT-PX1N9AWZ CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Limited eye motility from Duane anomaly Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Port-Wine Stain
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Left Isomerism
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Holoprosencephaly
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal coronary artery morphology
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Decreased projection of lower jaw
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal aortic morphology
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Pyloric Stenosis, Hypertrophic
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hand polydactyly
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital scar
Disease or Phenotype (Entity type)

KFPT:PT-PX1N9AWZ CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Limited eye motility from Duane anomaly
Disease or Phenotype (Entity type)

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