Hepatoencephalopathy Due To Combined Oxidative Phosphorylation Defect Type 1
| Disease Aliases (4) | Combined oxidative phosphorylation deficiency caused by mutation in gfm1 Combined oxidative phosphorylation deficiency type 1 Gfm1 combined oxidative phosphorylation deficiency Hepatoencephalopathy due to coxpd1 |
Associated Genes (0) | |||||||
| Cross-references of Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |