Multiple mitochondrial dysfunctions syndrome 9b

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Multiple mitochondrial dysfunctions syndrome
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Multiple mitochondrial dysfunctions syndrome 9B
MONDO_0971174
FDXR Causal
30250212 33348459 32499495 28965846 29040572 37046037 37481223
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Multiple mitochondrial dysfunctions syndrome 9b.
5 View disease cluster →
Optic atrophy mitochondrial dysfunction syndrome 1 shared geneFDXR Related via 1 shared gene including FDXR. Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome 1 shared geneFDXR Related via 1 shared gene including FDXR. Auditory neuropathy with optic atrophy 1 shared geneFDXR Related via 1 shared gene including FDXR. Auditory neuropathy 1 shared geneFDXR Related via 1 shared gene including FDXR. Optic atrophy 1 shared geneFDXR Related via 1 shared gene including FDXR.