Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4359
Gene Symbol: MPZ
MPZ
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		0.110 GeneticVariation BEFREE We found the association of a heterozygous novel MPZ gene point mutation, Ile62Phe in exon 2, with autosomal dominant motor and sensory neuropathy with focally folded myelin sheaths. 10214757

1999
Entrez Id: 4359
Gene Symbol: MPZ
MPZ
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		0.110 GeneticVariation CLINVAR