Pierre-Robin sequence (Phenotype)

Synonyms:Pierre Robin sequence, Pierre-robin anomaly, Pierre-robin deformity, Pierre-robin malformation, Robin sequence

Id:HP:0000201

Description:Pierre Robin malformation is a sequence of developmental malformations characterized by micrognathia (mandibular hypoplasia), glossoptosis and cleft palate.

Results found

Linked to

	Label	Description
	PT 6S1TFJ3D Subject (Entity type)	A subject from Kids First produced as part of the SD BHJXBDQK project
	PT 2Q72N8MG Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project
	PT G4YDY9AA Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project
	PT FHB01FDG Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project
	PT G4RRM1FF Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project
	PT HH76M8KZ Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project
	PT YTZPGNAF Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project
	PT DVA0ATVB Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project
	PT 4FX7SSPZ Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project
	PT 5EVSVDKQ Subject (Entity type)	A subject from Kids First produced as part of the SD 0TYVY1TW project

PT 6S1TFJ3D

Subject (Entity type)

A subject from Kids First produced as part of the SD BHJXBDQK project

PT 2Q72N8MG

Subject (Entity type)