congenital mirror movement disorder

Summary
Synonym
  • familial congenital controlateral synkinesia
  • familial congenital mirror movements
  • hereditary congenital controlateral synkinesia
  • hereditary congenital mirror movements
  • isolated congenital controlateral synkinesia
  • isolated congenital mirror movements
Definition
A movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs.
Super Class
movement disease physical disorder
External Links
Disease Ontology
DOID:0111153
ORDO
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1630 DCC DCC netrin 1 receptor
9423 NTN1 netrin 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
13176 Dcc DCC netrin 1 receptor
18208 Ntn1 netrin 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
25311 Dcc DCC netrin 1 receptor
Displaying all 2 entries
Gene ID Gene Symbol Description Source
32398 NetA Netrin-A
32400 NetB Netrin-B
Displaying all 2 entries
Gene ID Gene Symbol Description Source
172233 unc-40 Netrin receptor unc-40
180961 unc-6 Netrin unc-6

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024