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COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Autosomal dominant spastic paraplegia type 10

KIF5A KIF5A


COMMON
GENES
KIF5A



Citations in the biomedical literature:


Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
KIF5A
Autosomal dominant spastic paraplegia type 10



Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Autosomal dominant spastic paraplegia type 10

Synonym(s):
- CMT due to KIF5A mutation

Synonym(s):
- SPG10

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: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537482

No signs/symptoms info available.