Cytoscape Web
Click node...

Friedreich ataxia
2 OMIM references -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Autosomal dominant macrothrombocytopenia
Synonym(s):
- FA
- FRDA
Classification (Orphanet):
- Rare cardiac disease
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: childhood
Average age of death: adult
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
1 MeSH reference: D005621
Gene symbol UniProt reference OMIM reference
FXN Q16595606829
No signs/symptoms info available.