×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary Motor and Sensory Neuropathies
0.600
Biomarker
MGD
A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function.
30239779
2019
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary Motor and Sensory Neuropathies
0.600
Biomarker
MGD
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
22689911
2012
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary Motor and Sensory Neuropathies
0.600
Biomarker
MGD
Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
18326085
2008
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary Motor and Sensory Neuropathies
0.600
Biomarker
MGD
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
7581451
1995
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary Motor and Sensory Neuropathies
0.600
Biomarker
MGD
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
1384988
1992
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Neuropathy
0.300
Biomarker
MGD
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hypertrophic neuropathy of infancy
0.200
Biomarker
MGD
A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function.
30239779
2019
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary motor and sensory neuropathy, types I-IV
0.200
Biomarker
MGD
A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function.
30239779
2019
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Peroneal muscular atrophy (axonal type) (hypertrophic type)
0.200
Biomarker
MGD
A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function.
30239779
2019
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hypertrophic neuropathy of infancy
0.200
Biomarker
MGD
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
22689911
2012
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary motor and sensory neuropathy, types I-IV
0.200
Biomarker
MGD
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
22689911
2012
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Peroneal muscular atrophy (axonal type) (hypertrophic type)
0.200
Biomarker
MGD
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
22689911
2012
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hypertrophic neuropathy of infancy
0.200
Biomarker
MGD
Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
18326085
2008
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary motor and sensory neuropathy, types I-IV
0.200
Biomarker
MGD
Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
18326085
2008
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Peroneal muscular atrophy (axonal type) (hypertrophic type)
0.200
Biomarker
MGD
Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
18326085
2008
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Other sphingolipidosis
0.200
Biomarker
MGD
Heterozygous null mutation of myelin P0 protein enhances susceptibility to autoimmune neuritis targeting P0 peptide.
12616486
2003
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
0.200
Biomarker
MGD
Heterozygous null mutation of myelin P0 protein enhances susceptibility to autoimmune neuritis targeting P0 peptide.
12616486
2003
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Other sphingolipidosis
0.200
Biomarker
MGD
The role of macrophages in demyelinating peripheral nervous system of mice heterozygously deficient in p0.
11266447
2001
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
0.200
Biomarker
MGD
The role of macrophages in demyelinating peripheral nervous system of mice heterozygously deficient in p0.
11266447
2001
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hypertrophic neuropathy of infancy
0.200
Biomarker
MGD
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
7581451
1995
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary motor and sensory neuropathy, types I-IV
0.200
Biomarker
MGD
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
7581451
1995
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Peroneal muscular atrophy (axonal type) (hypertrophic type)
0.200
Biomarker
MGD
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
7581451
1995
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hypertrophic neuropathy of infancy
0.200
Biomarker
MGD
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
1384988
1992
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Hereditary motor and sensory neuropathy, types I-IV
0.200
Biomarker
MGD
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
1384988
1992
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Peroneal muscular atrophy (axonal type) (hypertrophic type)
0.200
Biomarker
MGD
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
1384988
1992