Search Ontology:
Human Disease
mirror movements 3
- Term ID
- DOID:0070639
- Synonyms
-
- Definition
- A congenital mirror movement disorder that has_material_basis_in homozygous mutation in the DNAL4 gene on chromosome 22q13. https://pubmed.ncbi.nlm.nih.gov/25098561/
- References
- Ontology
- Human Disease ( DOID:0070639 )
- is a type of
-
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Genes Involved
Zebrafish Models