Mirror movements

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MIRROR MOVEMENTS 1
157600MONDO:0008002OMIM:157600
DCC Causal
19720981 20431009 21242494 24808016 28250454 28341853
CTD, ClinVar, HPO
MIRROR MOVEMENTS 1 AND/OR AGENESIS OF THE CORPUS CALLOSUM
MONDO:0100515
DCC Causal
11335129 12451134 20431009 21242494 24808016 25813273 28250454 28250456 31697046 33141514 8861902 9126737 19720981 19127048
ClinGen, GWAS catalog
MIRROR MOVEMENTS 2
614508C3281089MONDO:0013790OMIM:614508
RAD51 Causal
22305526 24808016 25813273 279760 37308287
CTD, ClinVar, Disgenet, GWAS catalog, HPO
MIRROR MOVEMENTS 3
616059C4015124MONDO:0014478OMIM:616059
DNAL4 Causal
2509856 25236653
CTD, ClinVar, Disgenet, GenCC, HPO
MIRROR MOVEMENTS 4
618264C4748869MONDO:0032641
NTN1 Causal
28945198
CTD, ClinVar, Disgenet, HPO
All4 Causal4 Unknown4
Related Diseases Diseases that share the most curated genes with Mirror movements.
5 View disease cluster →
Congenital mirror movements 4 shared genesDCC, RAD51, NTN1, DNAL4 Related via 4 shared genes including DCC, RAD51, NTN1. Horizontal gaze palsy with progressive scoliosis 1 shared geneDCC Related via 1 shared gene including DCC. Partial agenesis of corpus callosum 1 shared geneDCC Related via 1 shared gene including DCC. Brain edema 1 shared geneNTN1 Related via 1 shared gene including NTN1. Hereditary breast and ovarian cancer syndrome 1 shared geneRAD51 Related via 1 shared gene including RAD51.