MPZ
myelin protein zero
Ассоциированные заболевания
Герминативная мутация (причина)7
Roussy-Lévy syndromeORPHA:3115
→Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic painORPHA:324585
→Dejerine-Sottas syndromeORPHA:64748
→Charcot-Marie-Tooth disease type 1BORPHA:101082
→Autosomal dominant intermediate Charcot-Marie-Tooth disease type DORPHA:100046
→Autosomal dominant Charcot-Marie-Tooth disease type 2IORPHA:99942
→Autosomal dominant Charcot-Marie-Tooth disease type 2JORPHA:99943
→Модифицирующая мутация1