Mitochondrial iron-sulfur cluster biogenesis

Pathway network for the Mitochondrial iron-sulfur cluster biogenesis SuperPath

Sources:
  • Reactome
  • WikiPathways

Gene overlap in member pathways for Mitochondrial iron-sulfur cluster biogenesis SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Mitochondrial iron-sulfur cluster biogenesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Covid-19Direct
2Multiple mitochondrial dysfunctions syndromeEnrichmentISCA1, ISCA26.07
3Combined oxidative phosphorylation deficiency 19EnrichmentLYRM4, NFS15.59
4Multiple mitochondrial dysfunctions syndrome 4EnrichmentISCA23.02
5Anemia, sideroblastic, 3, pyridoxine-refractoryEnrichmentGLRX53.02
6Myopathy with lactic acidosis, hereditaryEnrichmentISCU3.02
7Combined oxidative phosphorylation deficiency 52EnrichmentNFS13.02
8Spasticity, childhood-onset, with hyperglycinemiaEnrichmentGLRX53.02
9Anemia, sideroblastic, 5EnrichmentHSCB3.02
10Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndromeEnrichmentFDXR3.02
11Spinocerebellar ataxia, x-linked 6, with or without sideroblastic anemiaEnrichmentABCB72.96
12Even-plus syndromeEnrichmentHSPA92.96
13Anemia, sideroblastic, 4EnrichmentHSPA92.96
14Spastic paraplegia 93, autosomal recessiveEnrichmentNFU12.96
15X-linked sideroblastic anemia with ataxiaEnrichmentABCB72.96
16Multiple mitochondrial dysfunctions syndrome 5EnrichmentISCA12.72
17Multiple mitochondrial dysfunctions syndrome 1EnrichmentNFU12.66
18Autosomal recessive sideroblastic anemiaEnrichmentHSPA92.66
19Mitochondrial myopathy, episodic, with or without optic atrophy and reversible leukoencephalopathyEnrichmentFDX22.54
20Friedreich ataxiaEnrichmentFXN2.54
21Auditory neuropathy and optic atrophyEnrichmentFDXR2.54
22Multiple mitochondrial dysfunctions syndrome 9bEnrichmentFDXR2.54
23Spastic quadriplegic cerebral palsyEnrichmentISCA22.42
24Mitochondrial myopathyEnrichmentFDX21.98
25Auditory neuropathyEnrichmentFDXR1.61
26Optic atrophy plus syndromeEnrichmentISCA21.38

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