Leukodystrophy, adult-onset, autosomal dominant, without amyloid angiopathy

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Subtype of: Leukodystrophy
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • leukodystrophy, adult-onset, autosomal dominant, without amyloid angiopathy
MONDO_0008215
CST3 Unknown — ClinGen
  • leukodystrophy, adult-onset, autosomal dominant, without amyloid angiopathy
MONDO_0008215
LMNB1 Unknown
16951681 20301621 21225301 21909802 24357685 25527826 25655951 27159321 28334938 28716252 32910914
Open Targets
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Leukodystrophy, adult-onset, autosomal dominant, without amyloid angiopathy.
5 View disease cluster →
Acys amyloidosis 1 shared geneCST3 Related via 1 shared gene including CST3. Demyelinating leukodystrophy 1 shared geneLMNB1 Related via 1 shared gene including LMNB1. Microcephaly 26, primary, autosomal dominant 1 shared geneLMNB1 Related via 1 shared gene including LMNB1. Oral submucous fibrosis 1 shared geneCST3 Related via 1 shared gene including CST3. Leukodystrophy 1 shared geneCST3 Related via 1 shared gene including CST3.