Familial congenital mirror movements
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Hereditary congenital controlateral synkinesia Isolated congenital controlateral synkinesia Hereditary congenital mirror movements Familial congenital controlateral synkinesia Isolated congenital mirror movements |
| Number of Symptoms | 3 |
| OrphanetNr: | 238722 |
| OMIM Id: |
157600
614508 |
| ICD-10: |
|
| UMLs: |
|
| MeSH: |
|
| MedDRA: |
|
| Snomed: |
|
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant [Orphanet] |
| Age of onset: |
Neonatal Infancy [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Rare genetic movement disorder
-Rare genetic disease Rare movement disorder -Rare neurologic disease |
Symptom Information:
|
|
(HPO:0001335) | Bimanual synkinesia | 9 / 7739 | ||||
|
|
(HPO:0003829) | Incomplete penetrance | 85 / 7739 | ||||
|
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|