FOXP2, forkhead box P2, 93986

N. diseases: 165; N. variants: 32
Disease: Apraxias ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003635
Disease: Apraxias
Apraxias 		0.320 Biomarker group CTD_human Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. 27120335 2016
CUI: C0003635
Disease: Apraxias
Apraxias 		0.320 Biomarker group CTD_human Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. 17033973 2006
CUI: C0003635
Disease: Apraxias
Apraxias 		0.320 GeneticVariation group BEFREE Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. 16470794 2006
CUI: C0003635
Disease: Apraxias
Apraxias 		0.320 GeneticVariation group BEFREE The KE family is a large three-generational pedigree in which half of the members suffer from a verbal and orofacial dyspraxia in association with a point mutation in the FOXP2 gene. 12599277 2003