Gene: CERS3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 204219
Gene Symbol: CERS3
CERS3 		0.110 GeneticVariation disease BEFREE Using autozygosity mapping and exome sequencing, we have identified a homozygous missense mutation in CERS3 in patients with congenital ichthyosis characterized by collodion membranes at birth, generalized scaling of the skin, and mild erythroderma. 23549421 2013
Entrez Id: 204219
Gene Symbol: CERS3
CERS3 		0.110 Biomarker disease HPO