Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8974
Gene Symbol: P4HA2
P4HA2
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.120 GeneticVariation BEFREE More recently, in Chinese patients severe myopia (MYP25, OMIM:617238) has been linked to mutations in P4HA2 gene. 29364500

2018
Entrez Id: 8974
Gene Symbol: P4HA2
P4HA2
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.120 Biomarker BEFREE P4HA2 was identified as a novel causative gene for nonsyndromic high myopia. 25741866

2015