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

DNM2 RAB7A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DNM2
(0.65)
RAB7A



Citations in the biomedical literature:


Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
DNM2
Autosomal dominant Charcot-Marie-Tooth disease type 2B
RAB7A



Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal dominant Charcot-Marie-Tooth disease type 2B

Synonym(s):
- CMTDIB

Synonym(s):
- CMT2B

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.