All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01356 - Guillain-Barre syndrome, familial 139393 - 0 0 PMP22 - -
01248 CMT-1E Charcot-Marie-Tooth disease, type IE (CMT-1E) 118300 - 0 0 PMP22 - -
01247 CMT1A Charcot-Marie-Tooth disease, type IA (CMT1A) 118220 AD 1 0 PMP22 - -
01387 Dejerine-Sottas neuropathy, hypertrophic, Dejerine-Sottas (Dejerine-Sottas) 145900 - 39 20 EGR2, MPZ, PMP22, PRX - -
01467 HNPP neuropathy, hereditary, with liability pressure palsies (HNPP) 162500 - 24 4 PMP22 - -
01549 Roussy-Levy syndrome, Roussy-Levy 180800 - 2 1 MPZ, PMP22 - -
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