genetic disease (Disease)

Id:DOID:630

Description:A disease that has_material_basis_in genetic variations in the human genome.

Linked to

	Label	Description
	DISEASE DOID 630 Collection (Entity type)	DiseasePage Collection: Genetic Diseases, Inborn (DOID:630, FILE=tcrd_disease_DOID_000630.json)
	SU003684 Subject (Entity type)	A subject from Metabolomics produced as part of the PR002189 project
	SU002265 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001387 project
	SU004549 Subject (Entity type)	A subject from Metabolomics produced as part of the PR002783 project
	SU004557 Subject (Entity type)	A subject from Metabolomics produced as part of the PR002783 project
	SU004555 Subject (Entity type)	A subject from Metabolomics produced as part of the PR002783 project
	SU004550 Subject (Entity type)	A subject from Metabolomics produced as part of the PR002783 project
	SU004552 Subject (Entity type)	A subject from Metabolomics produced as part of the PR002783 project
	SU002666 Subject (Entity type)	A subject from Metabolomics produced as part of the PR001653 project
	SU004556 Subject (Entity type)	A subject from Metabolomics produced as part of the PR002783 project

DISEASE DOID 630

DiseasePage Collection: Genetic Diseases, Inborn (DOID:630, FILE=tcrd_disease_DOID_000630.json)

SU003684

A subject from Metabolomics produced as part of the PR002189 project

SU002265

A subject from Metabolomics produced as part of the PR001387 project

SU004549