Search Ontology:
Human Disease
mirror movements 2
- Term ID
- DOID:0070637
- Synonyms
-
- Definition
- A congenital mirror movement disorder that has_material_basis_in heterozygous mutation in the RAD51 gene on chromosome 15q15. https://pmc.ncbi.nlm.nih.gov/articles/PMC5099496/
- References
- Ontology
- Human Disease ( DOID:0070637 )
- is a type of
-
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Genes Involved
Zebrafish Models