Familial Congenital Mirror Movements

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Familial Congenital Mirror Movements

DCC
NTN1
DNAL4
RAD51

View recommended genes panels

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.

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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

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Sources and references

You can check the following sources for additional information.

ORPHANET OMIM Genetic Syndrome Finder

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