All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03781 CMT4F Charcot-Marie-Tooth disease, type 4F (CMT-4F) 614895 AR - - PRX - -
01387 DejerineSottas Dejerine-Sottas disease (hypertrophic neuropathy) 145900 AD;AR 39 20 EGR2, MPZ, PMP22, PRX - -
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