LPO, lactoperoxidase, 4025

N. diseases: 32; N. variants: 12
Disease: Meckel syndrome type 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1 		0.100 GeneticVariation disease CLINVAR Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online. 17397051 2007
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1 		0.100 GeneticVariation disease CLINVAR MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome. 16415886 2006
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1 		0.100 CausalMutation disease CLINVAR