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Charcot-Marie-Tooth disease type 4J
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Amyotrophic lateral sclerosis
Primary lateral sclerosis
Yunis-Varon syndrome
Synonym(s):
- CMT4J
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
FIG4 Q92562609390
No signs/symptoms info available.