ALX1, ALX homeobox 1, 8092

N. diseases: 59; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3150706
Disease: FRONTONASAL DYSPLASIA 3
FRONTONASAL DYSPLASIA 3
0.600 Biomarker disease GENOMICS_ENGLAND Aristaless-Like Homeobox protein 1 (ALX1) variant associated with craniofacial structure and frontonasal dysplasia in Burmese cats. 26610632 2016
CUI: C3150706
Disease: FRONTONASAL DYSPLASIA 3
FRONTONASAL DYSPLASIA 3
0.600 Biomarker disease GENOMICS_ENGLAND Defective neural crest migration revealed by a Zebrafish model of Alx1-related frontonasal dysplasia. 23059813 2013
CUI: C3150706
Disease: FRONTONASAL DYSPLASIA 3
FRONTONASAL DYSPLASIA 3
0.600 Biomarker disease GENOMICS_ENGLAND Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. 20451171 2010
CUI: C3150706
Disease: FRONTONASAL DYSPLASIA 3
FRONTONASAL DYSPLASIA 3
0.600 GermlineCausalMutation disease ORPHANET Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. 20451171 2010
CUI: C3150706
Disease: FRONTONASAL DYSPLASIA 3
FRONTONASAL DYSPLASIA 3
0.600 Biomarker disease GENOMICS_ENGLAND Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. 20451171 2010
CUI: C3150706
Disease: FRONTONASAL DYSPLASIA 3
FRONTONASAL DYSPLASIA 3
0.600 CausalMutation disease CLINVAR