Familial Congenital Mirror Movements
Genes related to Familial Congenital Mirror Movements
- DCC
- NTN1
- DNAL4
- RAD51
Clinical Features
Top most frequent phenotypes and symptoms related to Familial Congenital Mirror Movements
- Pain
- Intellectual disability, mild
- Agenesis of corpus callosum
- Myalgia
- Abnormality of movement
- Specific learning disability
- Clumsiness
- Situs inversus totalis
- Hypogonadotrophic hypogonadism
- Cerebral palsy
And another 6 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Familial Congenital Mirror Movements Is also known as hereditary congenital controlateral synkinesia, isolated congenital controlateral synkinesia, hereditary congenital mirror movements, isolated congenital mirror movements, familial congenital controlateral synkinesia.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Familial Congenital Mirror Movements Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Congenital mirror movements type 1 (deletion/duplication analysis of DCC gene).
By CGC Genetics (Portugal).
DCC
Specificity
100 %
Genes
25 % |
Congenital mirror movements type 1 (sequence analysis of DCC gene).
By CGC Genetics (Portugal).
DCC
Specificity
100 %
Genes
25 % |
Congenital mirror movements type 1 (deletion/duplication analysis of DCC gene).
By CGC Genetics (Portugal).
DCC
Specificity
100 %
Genes
25 % |
Congenital mirror movements type 1 (sequence analysis of DCC gene).
By CGC Genetics (Portugal).
DCC
Specificity
100 %
Genes
25 % |
Mirror movements type 1.
By Centogene AG - the Rare Disease Company (Germany).
DCC
Specificity
100 %
Genes
25 % |
Esophageal carcinoma, somatic.
By Centogene AG - the Rare Disease Company (Germany).
DCC
Specificity
100 %
Genes
25 % |
Colorectal cancer, somatic.
By Centogene AG - the Rare Disease Company (Germany).
DCC
Specificity
100 %
Genes
25 % |
Single gene testing DCC.
By CeGaT GmbH (Germany).
DCC
Specificity
100 %
Genes
25 % |
You can get up to 32 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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