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Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Dedifferentiated liposarcoma
3 associated genes
No signs/symptoms info
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Dedifferentiated liposarcoma

KIF5A
(UniProt - OMIM)
 CDK4
(UniProt - OMIM)
HMGA2
(UniProt - OMIM)
MDM2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KIF5A
(0.49)
MDM2


Citations in the biomedical literature:


Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
KIF5A
Dedifferentiated liposarcoma
CDK4 HMGA2 MDM2



Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Dedifferentiated liposarcoma

Synonym(s):
- CMT due to KIF5A mutation
Synonym(s):
- DDLS
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.