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

KIF5A
(UniProt - OMIM)
 KIF5A
(UniProt - OMIM)

COMMON
GENES 		KIF5A


Citations in the biomedical literature:


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



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

Synonym(s):
- SPG10
Synonym(s):
- CMT due to KIF5A mutation
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: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C537482
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.