All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01387 - Dejerine-Sottas disease 145900 - - - EGR2, MPZ, PMP22, PRX - -
01549 - Roussy-Levy syndrome 180800 - - - MPZ, PMP22 - -
02535 CHN neuropathy, hypomyelinating, congenital (CHN) 605253 - - - EGR2, MPZ - -
01245 CMT-1B Charcot-Marie-Tooth disease, type IB (CMT-1B) 118200 - - - MPZ - -
02689 CMT-2I Charcot-Marie-Tooth disease, type 2I (CMT-2I) 607677 - - - MPZ - -
02699 CMT-2J Charcot-Marie-Tooth disease, type 2J (CMT-2J) 607736 - - - MPZ - -
02704 CMTDID Charcot-Marie-Tooth disease, dominant intermediate, type D (CMTDID) 607791 - - - MPZ - -
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