MSeqDR Mitochondrial Disease Portal


 
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  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
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expandleukodystrophy (MONDO:0019046)
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expandmitochondrial oxidative phosphorylation disorder with no known mechanism (MONDO:0016799)
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expandrare hereditary metabolic disease with peripheral neuropathy (MONDO:0016133)
..Starting node
..expandnon-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy ()

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..expandLeigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome ()  LSDB  L: 00525;
..expandlong chain 3-hydroxyacyl-CoA dehydrogenase deficiency ()  LSDB  L: 00474;
..expandmetachromatic leukodystrophy ()
..expandmethylmalonic aciduria and homocystinuria type cblC ()
..expandmitochondrial disease with peripheral neuropathy ()
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..expandnon-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy ()
..expandoptic atrophy-peripheral neuropathy-developmental delay syndrome ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:18576
Name:non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy
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Reference: MedGen:
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