Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54499
Gene Symbol: TMCO1
TMCO1
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.430 Biomarker CTD_human Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation. 20018682

2010