Multiple system atrophy

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MULTIPLE SYSTEM ATROPHY
MESH:D019578MONDO:0007803
COQ2 Causal — CTD, GenCC
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MONDO:0020715
COQ2 Causal — ClinVar
MULTIPLE SYSTEM ATROPHY, CEREBELLAR TYPE
C5554234
MFN2 Causal — Disgenet
All30 Causal2 Unknown29
Related Diseases Diseases that share the most curated genes with Multiple system atrophy.
5 View disease cluster →
Developmental dysplasia of the hip 2 shared genesLOXL4, PYROXD2 Related via 2 shared genes including LOXL4, PYROXD2. Axonal hereditary motor and sensory neuropathy 1 shared geneMFN2 Related via 1 shared gene including MFN2. multiple symmetric lipomatosis with partial lipodystrophy 1 shared geneMFN2 Related via 1 shared gene including MFN2. Charcot-Marie-Tooth disease type 2A2 1 shared geneMFN2 Related via 1 shared gene including MFN2. nail-patella syndrome 1 shared geneLMX1B Related via 1 shared gene including LMX1B.