All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02535 CHN1 neuropathy, hypomyelinating, congenital, type 1 605253 AD;AR 2 2 EGR2, MPZ - -
02690 CMT1D Charcot-Marie-Tooth disease, type ID (CMT-1D) 607678 AD 1 1 EGR2 - -
01387 DejerineSottas Dejerine-Sottas disease (hypertrophic neuropathy) 145900 AD;AR 39 20 EGR2, MPZ, PMP22, PRX - -
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