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Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Charcot-Marie-Tooth disease type 1B
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Charcot-Marie-Tooth disease type 1B

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

COMMON
GENES 		MPZ


Citations in the biomedical literature:


Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
MPZ
Charcot-Marie-Tooth disease type 1B



Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Charcot-Marie-Tooth disease type 1B

Synonym(s):
- CMTDID
Synonym(s):
- CMT1B
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: childhood
Average age of death: young adult
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.