Peeling skin syndromeGene: KRT2
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Ichthyosis bullosa of Siemens, 146800; blistering, superficial peeling of the skin, and localized lichenified hyperkeratosis
12 December 2016: Reviews were assessed, and panel was revised according to expert review and additional curation.
KRT2 was created by rfoulger
KRT2 was added to Peeling skin syndromepanel. Sources: Other