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
01247 CMT1A Charcot-Marie-Tooth disease, type IA (CMT1A) 118220 AD 1 - PMP22 - -
01248 CMT1E Charcot-Marie-Tooth disease, type IE (CMT-1E) 118300 AD - - PMP22 - -
01387 DejerineSottas Dejerine-Sottas disease (hypertrophic neuropathy) 145900 AD;AR 39 20 EGR2, MPZ, PMP22, PRX - -
01356 GBS Guillain-Barre syndrome, familial 139393 - - - PMP22 - -
01467 HNPP neuropathy, hereditary, with liability pressure palsies (HNPP) 162500 AD 24 4 PMP22 - -
01549 Roussy-Levy syndrome Roussy-Levy syndrome 180800 AD 2 1 MPZ, PMP22 - -
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