FLG2, filaggrin family member 2, 388698

N. diseases: 14; N. variants: 4
Disease: PEELING SKIN SYNDROME 3 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4015729
Disease: PEELING SKIN SYNDROME 3
PEELING SKIN SYNDROME 3 		0.300 GermlineCausalMutation disease ORPHANET Peeling skin syndrome associated with novel variant in FLG2 gene. 28884927 2017