Hepatoencephalopathy due to combined oxidative phosphorylation defect

Disease Term Disease ID Gene Symbol Classification References Source
HEPATOENCEPHALOPATHY DUE TO COMBINED OXIDATIVE PHOSPHORYLATION DEFECT TYPE 1
137681C4707239MONDO:0012191
GFM1 Causal
17160893 23430926
ClinVar Disgenet GWAS catalog Orphanet