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KFPT:PT-T8YKNXD4 CUI (Kfpt)

Kfpt:PT-T8YKNXD4

Id:0ec5f6f0-9f78-5dd1-876c-9cf6bd2a3722

Results found

Linked to

	Label	Description
	KFPT:PT-T8YKNXD4 CUI has phenotype Abnormal connection between trachea and esophagus Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI has phenotype Wolff-Parkinson-White Syndrome Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI has phenotype Cardiomyopathies Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI has phenotype Congenital atresia of rectum Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI has phenotype Pierre Robin Syndrome Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI has phenotype Tetralogy of Fallot Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI has phenotype Cleft lip Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI has phenotype Hypoplastic Left Heart Syndrome Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI belongs to cohort Kids First: Esophageal Atresia and Tracheoesophageal Fistulas Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-T8YKNXD4 CUI has phenotype Congenital anomaly of face Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Abnormal connection between trachea and esophagus

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Wolff-Parkinson-White Syndrome

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Cardiomyopathies

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Congenital atresia of rectum

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Pierre Robin Syndrome

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Tetralogy of Fallot

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Cleft lip

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Hypoplastic Left Heart Syndrome

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI belongs to cohort Kids First: Esophageal Atresia and Tracheoesophageal Fistulas

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-T8YKNXD4 CUI has phenotype Congenital anomaly of face

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

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@CFDE Workbench 2026

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.

Consortium

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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 2026

This repository is under review for potential modification in compliance with Administration directives.