KFPT:PT-PGH7V33R CUI (KFPT)

Description: A kfpt in the knowledge graph

Analyze

CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View KFPT:PT-PGH7V33R CUI's neighborhood in the knowledge graph.

Submit

Knowledge Graph Assertions

Source	Relation	Target
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal palate morphology Disease or Phenotype (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Facial Paresis Disease or Phenotype (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Scoliosis, unspecified Disease or Phenotype (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Lower cranial nerve dysfunction Disease or Phenotype (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital digestive system anomalies Disease or Phenotype (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Phenotypic abnormality Disease or Phenotype (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Belongs to cohort Knowledge Graph Relation (Entity type)	Kids First: Syndromic Cranial Dysinnervation KFCOHORT (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Cardiovascular Abnormalities Disease or Phenotype (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital anomaly of face Disease or Phenotype (Entity type)
KFPT:PT-PGH7V33R CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Imaging of brain abnormal Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal palate morphology
Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Facial Paresis
Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Scoliosis, unspecified
Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Lower cranial nerve dysfunction
Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital digestive system anomalies
Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Phenotypic abnormality
Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Belongs to cohort
Knowledge Graph Relation (Entity type)
Kids First: Syndromic Cranial Dysinnervation
KFCOHORT (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Cardiovascular Abnormalities
Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital anomaly of face
Disease or Phenotype (Entity type)

KFPT:PT-PGH7V33R CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Imaging of brain abnormal
Disease or Phenotype (Entity type)

DISPLAY PER PAGE

CFDE Workbench

Consortium

Community

Resources

@CFDE Workbench 2025

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.