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KFPT:PT-1FPQSQCV CUI (Kfpt)

Kfpt:PT-1FPQSQCV

Id:c98723f5-a915-5a2a-b713-47d7070f62f6

Results found

Linked to

	Label	Description
	KFPT:PT-1FPQSQCV CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Imaging of brain abnormal Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Facial Paresis Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Phenotypic abnormality Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Congenital digestive system anomalies Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Urogenital Diseases Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Congenital anomaly of face Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Hearing abnormality Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Limited extraocular movements Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-1FPQSQCV CUI has phenotype Cardiovascular Abnormalities Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Imaging of brain abnormal

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Facial Paresis

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Phenotypic abnormality

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Congenital digestive system anomalies

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Urogenital Diseases

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Congenital anomaly of face

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Hearing abnormality

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Limited extraocular movements

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-1FPQSQCV CUI has phenotype Cardiovascular Abnormalities

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.