Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4512
Gene Symbol: COX1
COX1
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		0.600 CausalMutation CLINVAR A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness. 8019558

1994