KFPT:PT-3G1M6632 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-3G1M6632 CUI's neighborhood in the knowledge graph.

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Knowledge Graph Assertions

Source	Relation	Target
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Sandal gap Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital malrotation of intestine Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hernia, Inguinal Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hand polydactyly Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Craniosynostosis Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Accessory nipple Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Microcephaly (physical finding) Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Asplenia Syndrome Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Retinal vascular tortuosity Disease or Phenotype (Entity type)
KFPT:PT-3G1M6632 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Left Isomerism Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Sandal gap
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital malrotation of intestine
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hernia, Inguinal
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hand polydactyly
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Craniosynostosis
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Accessory nipple
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Microcephaly (physical finding)
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Asplenia Syndrome
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Retinal vascular tortuosity
Disease or Phenotype (Entity type)

KFPT:PT-3G1M6632 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Left Isomerism
Disease or Phenotype (Entity type)

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