Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.700 Biomarker disease GENOMICS_ENGLAND A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations. 29215649 2018
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.700 GeneticVariation disease UNIPROT Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. 11137991 2001
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.700 GeneticVariation disease UNIPROT The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). 11106354 2000
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.700 Biomarker disease CTD_human
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.700 CausalMutation disease CLINVAR