Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8092
Gene Symbol: ALX1
ALX1
CUI: C0432106
Disease: Midline facial cleft - Tessier cleft 0
Midline facial cleft - Tessier cleft 0 		0.020 GeneticVariation BEFREE Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia. 27324866

2017
Entrez Id: 8092
Gene Symbol: ALX1
ALX1
CUI: C0432106
Disease: Midline facial cleft - Tessier cleft 0
Midline facial cleft - Tessier cleft 0 		0.020 GeneticVariation BEFREE Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. 20451171

2010