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KFPT:PT-AXN0W87J 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-AXN0W87J CUI's neighborhood in the knowledge graph.

Knowledge Graph Assertions

	Source	Relation	Target	Evidence
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Cardiovascular Abnormalities Disease or Phenotype (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Urogenital Diseases Disease or Phenotype (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital digestive system anomalies Disease or Phenotype (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hearing abnormality Disease or Phenotype (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Phenotypic abnormality Disease or Phenotype (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Limited extraocular movements Disease or Phenotype (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital anomaly of face Disease or Phenotype (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Imaging of brain abnormal Disease or Phenotype (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Belongs to cohort Knowledge Graph Relation (Entity type)	Kids First: Syndromic Cranial Dysinnervation KFCOHORT (Entity type)
	KFPT:PT-AXN0W87J CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Facial Paresis Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Cardiovascular Abnormalities
Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Urogenital Diseases
Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital digestive system anomalies
Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hearing abnormality
Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Phenotypic abnormality
Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Limited extraocular movements
Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital anomaly of face
Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Imaging of brain abnormal
Disease or Phenotype (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Belongs to cohort
Knowledge Graph Relation (Entity type)
Kids First: Syndromic Cranial Dysinnervation
KFCOHORT (Entity type)

KFPT:PT-AXN0W87J CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Facial Paresis
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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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