KFPT:PT-P0GR43XW 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-P0GR43XW CUI's neighborhood in the knowledge graph.

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Knowledge Graph Assertions

Source	Relation	Target
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Lower cranial nerve dysfunction Disease or Phenotype (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Imaging of brain abnormal Disease or Phenotype (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal palate morphology Disease or Phenotype (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Belongs to cohort Knowledge Graph Relation (Entity type)	Kids First: Syndromic Cranial Dysinnervation KFCOHORT (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital anomaly of face Disease or Phenotype (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hearing abnormality Disease or Phenotype (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Facial Paresis Disease or Phenotype (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Urogenital Diseases Disease or Phenotype (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital digestive system anomalies Disease or Phenotype (Entity type)
KFPT:PT-P0GR43XW CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Limited extraocular movements Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Lower cranial nerve dysfunction
Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Imaging of brain abnormal
Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal palate morphology
Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Belongs to cohort
Knowledge Graph Relation (Entity type)
Kids First: Syndromic Cranial Dysinnervation
KFCOHORT (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital anomaly of face
Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hearing abnormality
Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Facial Paresis
Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Urogenital Diseases
Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital digestive system anomalies
Disease or Phenotype (Entity type)

KFPT:PT-P0GR43XW CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Limited extraocular movements
Disease or Phenotype (Entity type)

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