CCNF gene related symptoms and diseases
All the information presented here about the CCNF gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,ORPHANET,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to CCNF gene
|Symptoms // Phenotype||% Cases|
|Microcephaly||Very Common - Between 80% and 100% cases|
|Xerostomia||Very Common - Between 80% and 100% cases|
|Peripheral demyelination||Very Common - Between 80% and 100% cases|
|Fasciculations||Very Common - Between 80% and 100% cases|
|Sleep apnea||Very Common - Between 80% and 100% cases|
Other less frequent symptoms and clinical featuresPatients with CCNF gene alterations may also develop some of the following symptoms and phenotypes:
Commonly - More than 50% cases
- Slurred speech
- Emotional lability
- Amyotrophic lateral sclerosis
- Bulbar palsy
- Muscle fibrillation
- Frontotemporal dementia
And 34 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to CCNF gene
Here you will find a list of rare diseases related to the CCNF. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
AMYOTROPHIC LATERAL SCLEROSIS
AMYOTROPHIC LATERAL SCLEROSIS Is also known as als, amyotrophic lateral sclerosis 1, autosomal dominant, fals, lou gehrig disease, charcot disease, amyotrophic lateral sclerosis 1, familial
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord.
Most common symptoms of AMYOTROPHIC LATERAL SCLEROSIS
- Muscle weakness
More info about AMYOTROPHIC LATERAL SCLEROSIS
Search interest in CCNF
Potential gene panels for CCNF gene
By Fulgent Genetics Fulgent Genetics
This panel specifically test the CCNF gene.More info about this panel
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