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KFPT:PT-QZT1XVPE CUI (Kfpt)

Kfpt:PT-QZT1XVPE

Id:85f841ce-dcfe-5da0-8f43-178c83051f16

Results found

Linked to

	Label	Description
	KFPT:PT-QZT1XVPE CUI has phenotype Congenital digestive system anomalies Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI has phenotype Congenital anomaly of face Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI has phenotype Cardiovascular Abnormalities Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI has phenotype Facial Paresis Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI has phenotype Lower cranial nerve dysfunction Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI has phenotype Hearing abnormality Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI has phenotype Urogenital Diseases Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI has phenotype Limited extraocular movements Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First
	KFPT:PT-QZT1XVPE CUI has phenotype Scoliosis, unspecified Knowledge Graph Assertion (Entity type)	A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE CUI has phenotype Congenital digestive system anomalies

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE CUI has phenotype Congenital anomaly of face

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE CUI has phenotype Cardiovascular Abnormalities

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE CUI has phenotype Facial Paresis

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE 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-QZT1XVPE CUI has phenotype Lower cranial nerve dysfunction

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE CUI has phenotype Hearing abnormality

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE CUI has phenotype Urogenital Diseases

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE CUI has phenotype Limited extraocular movements

Knowledge Graph Assertion (Entity type)

A Knowledge Graph Assertion from Kids First

Knowledge Graph Assertion

KFPT:PT-QZT1XVPE CUI has phenotype Scoliosis, unspecified

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

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