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- Campomelic Dysplasia
Campomelic dysplasia
- Other Names:
CMD1; CMPD; CMPD1; CMPD1/SRA1CMD1; CMPD; CMPD1; CMPD1/SRA1
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This section is currently in development.
Many rare diseases have limited information. Currently GARD is able to provide the following information for this disease:
38 Symptoms
Campomelic dysplasia is a genetic disease, which means that it is caused by one or more genes not working correctly.
The following gene(s) are known to be associated with this disease: SOX9
Questions:
All individuals inherit two copies of most genes. The number of copies of a gene that need to have a disease-causing variant affects the way a disease is inherited. This disease is inherited in the following pattern(s):
Questions:
Last Updated: Nov. 8, 2021