KFPT:PT-QH7GYQTX 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-QH7GYQTX CUI's neighborhood in the knowledge graph.

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Knowledge Graph Assertions

Source	Relation	Target
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Sandal gap Disease or Phenotype (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Arnold Chiari Malformation Disease or Phenotype (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Spinal fusion Disease or Phenotype (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital blindness Disease or Phenotype (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Renal dysplasia Disease or Phenotype (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Belongs to cohort Knowledge Graph Relation (Entity type)	Kids First: Congenital Heart Defects KFCOHORT (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hypoplastic Left Heart Syndrome Disease or Phenotype (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Retinal vascular tortuosity Disease or Phenotype (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Holoprosencephaly Disease or Phenotype (Entity type)
KFPT:PT-QH7GYQTX CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Branchioma Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Sandal gap
Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Arnold Chiari Malformation
Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Spinal fusion
Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital blindness
Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Renal dysplasia
Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Belongs to cohort
Knowledge Graph Relation (Entity type)
Kids First: Congenital Heart Defects
KFCOHORT (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hypoplastic Left Heart Syndrome
Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Retinal vascular tortuosity
Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Holoprosencephaly
Disease or Phenotype (Entity type)

KFPT:PT-QH7GYQTX CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Branchioma
Disease or Phenotype (Entity type)

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