KRT14
keratin 14
Ассоциированные заболевания
Герминативная мутация (причина)7
Naegeli-Franceschetti-Jadassohn syndromeORPHA:69087
→Dermatopathia pigmentosa reticularisORPHA:86920
→Autosomal recessive generalized epidermolysis bullosa simplexORPHA:89838
→Autosomal dominant generalized epidermolysis bullosa simplex, severe formORPHA:79396
→Epidermolysis bullosa simplex with mottled pigmentationORPHA:79397
→Autosomal dominant generalized epidermolysis bullosa simplex, intermediate formORPHA:79399
→Localized epidermolysis bullosa simplexORPHA:79400
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