Pelizaeus-merzbacher disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
PELIZAEUS-MERZBACHER DISEASE
C0205711312080MESH:D020371
GJC2 Causal — Disgenet
PLP1 Causal
18571143
CTD, ClinVar, Disgenet, HPO —
PELIZAEUS-MERZBACHER DISEASE, ATYPICAL
C0751915
PLP1 Causal — Disgenet —
All6 Causal2 Unknown6
Related Diseases Diseases that share the most curated genes with Pelizaeus-merzbacher disease.
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Spastic paraplegia, x-linked 2 shared genesPLP1, RAB9B Related via 2 shared genes including PLP1, RAB9B. hypomyelinating leukodystrophy 3 1 shared geneAIMP1 Related via 1 shared gene including AIMP1. hypomyelinating leukodystrophy 2 1 shared geneGJC2 Related via 1 shared gene including GJC2. Hypomyelinating leukodystrophy 4 shared genesAIMP1, HSPD1, GJC2, MAL Related via 4 shared genes including AIMP1, HSPD1, GJC2. Metachromatic leukodystrophy 1 shared geneMAL Related via 1 shared gene including MAL.