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Familial congenital mirror movements
2 OMIM references -
2 associated genes
57 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary breast and ovarian cancer syndrome
Familial pancreatic carcinoma
Fanconi anemia
Hereditary breast cancer
Blackfan-Diamond anemia
Cree leukoencephalopathy
Ovarioleukodystrophy
Familial prostate cancer
Hereditary site-specific ovarian cancer syndrome
Precursor B-cell acute lymphoblastic leukemia
B-cell chronic lymphocytic leukemia
Constitutional mismatch repair deficiency syndrome
Hereditary nonpolyposis colon cancer
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Bloom syndrome
Chronic myeloid leukemia
Precursor T-cell acute lymphoblastic leukemia
Adrenocortical carcinoma
Alpha-thalassemia - X-linked intellectual deficit syndrome
Alpha-thalassemia - myelodysplastic syndrome
Carpenter-Waziri syndrome
Chudley-Lowry-Hoar syndrome
Essential thrombocythemia
Giant cell glioblastoma
Gliosarcoma
Holmes-Gang syndrome
Juberg-Marsidi syndrome
Li-Fraumeni syndrome
Papilloma of choroid plexus
Primary peritoneal carcinoma
Smith-Fineman-Myers syndrome
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism
Autosomal recessive primary microcephaly
Premature chromosome condensation with microcephaly and intellectual deficit
Werner syndrome
Ataxia-telangiectasia
Ataxia-telangiectasia variant
Combined cervical dystonia
Mantle cell lymphoma
Congenital analbuminemia
Distal 22q11.2 microdeletion syndrome
Acute promyelocytic leukemia
Amyotrophic lateral sclerosis
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Hyper-IgM syndrome type 2
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Pulverulent cataract
COFS syndrome
Trichothiodystrophy
Xeroderma pigmentosum complementation group D
Synonym(s):
- Familial congenital controlateral synkinesia
- Hereditary congenital controlateral synkinesia
- Hereditary congenital mirror movements
- Isolated congenital controlateral synkinesia
- Isolated congenital mirror movements
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
DCC P43146120470
RAD51 Q06609179617
No signs/symptoms info available.