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Autosomal dominant Charcot-Marie-Tooth disease type 2J
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Charcot-Marie-Tooth disease type 1E
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant Charcot-Marie-Tooth disease type 2J
Charcot-Marie-Tooth disease type 1E

MPZ
(UniProt - OMIM)
 PMP22
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MPZ
(0.94)
PMP22


Citations in the biomedical literature:


Autosomal dominant Charcot-Marie-Tooth disease type 2J
MPZ
Charcot-Marie-Tooth disease type 1E
PMP22



Autosomal dominant Charcot-Marie-Tooth disease type 2J
Charcot-Marie-Tooth disease type 1E

Synonym(s):
- CMT2J
Synonym(s):
- CMT1E
- Charcot-Marie-Tooth disease - deafness
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare otorhinolaryngologic disease
Classification (ICD10):
- Diseases of the nervous system -
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
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
2 MeSH references: C537986 / C538078
No signs/symptoms info available.