Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7051
Gene Symbol: TGM1
TGM1
CUI: C0079154
Disease: Congenital Nonbullous Ichthyosiform Erythroderma
Congenital Nonbullous Ichthyosiform Erythroderma 		1.000 GermlineCausalMutation ORPHANET Inherited ichthyoses/generalized Mendelian disorders of cornification. 22739337

2013
Entrez Id: 7051
Gene Symbol: TGM1
TGM1
CUI: C0079154
Disease: Congenital Nonbullous Ichthyosiform Erythroderma
Congenital Nonbullous Ichthyosiform Erythroderma 		1.000 GermlineCausalMutation ORPHANET Mutations in any of the three known causative genes, TGM1, ALOXE3 or ALOX12B, can lead either to NBCIE or LI. 12780701

2003