Cytoscape Web
Click node...

Charcot-Marie-Tooth disease type 2H
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
1 OMIM reference -
1 associated gene
No signs/symptoms info
Charcot-Marie-Tooth disease type 2H
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A

GDAP1
(UniProt - OMIM)
 GDAP1
(UniProt - OMIM)

COMMON
GENES 		GDAP1


Citations in the biomedical literature:


Charcot-Marie-Tooth disease type 2H
GDAP1
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A



Charcot-Marie-Tooth disease type 2H
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A

Synonym(s):
- AR-CMT2C
- Autosomal recessive axonal CMT4C2
- Axonal Charcot-Marie-Tooth disease with pyramidal involvement
Synonym(s):
- RI-CMT type A
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: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: C535415
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.