Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.100 CausalMutation phenotype CLINVAR Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. 26805781 2016