SLC25A32 gene related symptoms and diseases
All the information presented here about the SLC25A32 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE,ORPHANET,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to SLC25A32 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Exercise intolerance | Uncommon - Between 30% and 50% cases |
| Ragged-red muscle fibers | Uncommon - Between 30% and 50% cases |
Rare diseases associated to SLC25A32 gene
Here you will find a list of rare diseases related to the SLC25A32. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE; RREI
Most common symptoms of EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE; RREI
- Exercise intolerance
- Ragged-red muscle fibers
More info about EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE; RREI
SOURCES: OMIM
MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY, MILD TYPE
Alternate names
MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY, MILD TYPE Is also known as mad deficiency, mild type, glutaric aciduria type 2, mild type, madd, mild type
More info about MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY, MILD TYPE
SOURCES: ORPHANET
Search interest in SLC25A32
Potential gene panels for SLC25A32 gene
SLC25A32 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the SLC25A32 gene.
More info about this panel United States.
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