Entrez Id: |
4359 |
Gene Symbol: |
MPZ |
MPZ
|
Neuropathy
|
0.300 |
Biomarker |
MGD |
|
|
|
Entrez Id: |
4359 |
Gene Symbol: |
MPZ |
MPZ
|
Dejerine-Sottas Disease (disorder)
|
1.000 |
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
|
Charcot-Marie-Tooth Disease, Type Ib
|
1.000 |
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
|
Roussy-Levy Syndrome (disorder)
|
0.900 |
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
|
Charcot-Marie-Tooth Disease
|
0.700 |
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 Type I
|
0.700 |
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 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
|
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 |
Entrez Id: |
4359 |
Gene Symbol: |
MPZ |
MPZ
|
Dejerine-Sottas Disease (disorder)
|
1.000 |
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
|
Charcot-Marie-Tooth Disease, Type Ib
|
1.000 |
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
|
Roussy-Levy Syndrome (disorder)
|
0.900 |
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
|
Charcot-Marie-Tooth Disease
|
0.700 |
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 Type I
|
0.700 |
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 |
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 |
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
|
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
|
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
|
Dejerine-Sottas Disease (disorder)
|
1.000 |
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
|
Charcot-Marie-Tooth Disease, Type Ib
|
1.000 |
Biomarker |
MGD |
Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
|
18326085 |
2008 |