Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551675
Disease: Keratoderma, Palmoplantar
Keratoderma, Palmoplantar
0.110 GeneticVariation disease BEFREE A group of hereditary palmoplantar keratodermas due to heterozygous mutation in the loricrin gene has recently been identified. 11703298 2001
CUI: C4551675
Disease: Keratoderma, Palmoplantar
Keratoderma, Palmoplantar
0.110 Biomarker disease HPO