Gene: ECM1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1893
Gene Symbol: ECM1
ECM1 		0.110 GeneticVariation phenotype BEFREE Lipoid proteinosis is a rare autosomal recessive disease characterized by cutaneous and mucosal lesions and hoarseness appearing in early childhood that is caused by homozygous or compound heterozygous mutations in the ECM1 gene located on chromosome 1q21. 21791056 2011
Entrez Id: 1893
Gene Symbol: ECM1
ECM1 		0.110 Biomarker phenotype HPO