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Autosomal dominant Charcot-Marie-Tooth disease type 2J
1 OMIM reference -
1 associated gene
10 connected diseases
No signs/symptoms info
Disease Type of connection
Dejerine-Sottas syndrome
Roussy-Lévy syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2I
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
Charcot-Marie-Tooth disease type 1B
Acute inflammatory demyelinating polyradiculoneuropathy
Charcot-Marie-Tooth disease type 1A
Charcot-Marie-Tooth disease type 1E
Hereditary neuropathy with liability to pressure palsies
Synonym(s):
- CMT2J
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MPZ P25189159440
No signs/symptoms info available.