KRT9, keratin 9, 3857

N. diseases: 30; N. variants: 14
Disease: Hyperkeratosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0870082
Disease: Hyperkeratosis
Hyperkeratosis 		0.020 GeneticVariation disease BEFREE Mutations in the keratin 9 gene (KRT9) have been shown to cause epidermolytic palmoplantar keratoderma (EPPK; OMIM 144200), an autosomal dominant genodermatosis characterized clinically by diffuse hyperkeratosis limited to the palms and soles, and histologically by epidermolysis in suprabasal layers of the epidermis. 19874353 2010
CUI: C0870082
Disease: Hyperkeratosis
Hyperkeratosis 		0.020 Biomarker disease BEFREE The epidermis showed hyperkeratosis and acanthosis by histologic studies and stained positively for keratin 9 in all of the suprabasal keratinocyte layers like palmoplantar-type skin. 11346340 2001