Monomelic amyotrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
AMYOTROPHY, HEREDITARY NEURALGIC
162100C1834304
SEPTIN9 Unknown — Disgenet, HPO
AMYOTROPHY, MONOMELIC
C1865384
ARPP21 Unknown — Disgenet —
CEP126 Unknown — Disgenet —
CPLANE1 Unknown — Disgenet —
RYR3 Unknown — Disgenet
SLIT1 Unknown — Disgenet
All6 Causal0 Unknown6
Related Diseases Diseases that share the most curated genes with Monomelic amyotrophy.
5 View disease cluster →
Neuralgic amyotrophy 1 shared geneSEPTIN9 Related via 1 shared gene including SEPTIN9. Brachial plexus neuritis 1 shared geneSEPTIN9 Related via 1 shared gene including SEPTIN9. joubert syndrome 17 1 shared geneCPLANE1 Related via 1 shared gene including CPLANE1. Encephalocele 1 shared geneCPLANE1 Related via 1 shared gene including CPLANE1. Hydrops fetalis 1 shared geneRYR3 Related via 1 shared gene including RYR3.