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Autosomal dominant Charcot-Marie-Tooth disease type 2E
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Young adult-onset Parkinsonism
14 OMIM references -
13 associated genes
No signs/symptoms info
Autosomal dominant Charcot-Marie-Tooth disease type 2E
Young adult-onset Parkinsonism

NEFL
(UniProt - OMIM)
 EIF4G1
(UniProt - OMIM)
GBA
(UniProt - OMIM)
GIGYF2
(UniProt - OMIM)
HTRA2
(UniProt - OMIM)
LRRK2
(UniProt - OMIM)
NR4A2
(UniProt - OMIM)
PACRG
(UniProt - OMIM)
PARK2
(UniProt - OMIM)
PARK7
(UniProt - OMIM)
PINK1
(UniProt - OMIM)
SNCA
(UniProt - OMIM)
UCHL1
(UniProt - OMIM)
VPS35
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NEFL
(0.63)
PARK2


Citations in the biomedical literature:


Autosomal dominant Charcot-Marie-Tooth disease type 2E
NEFL
Young adult-onset Parkinsonism
EIF4G1 GBA GIGYF2 HTRA2 LRRK2 NR4A2
PACRG PARK2 PARK7 PINK1 SNCA UCHL1
VPS35



Autosomal dominant Charcot-Marie-Tooth disease type 2E
Young adult-onset Parkinsonism

Synonym(s):
- CMT2E
Synonym(s):
- Early-onset Parkinson disease
- Familial Parkinson disease
- Hereditary Parkinson disease
- Young-onset Parkinson disease
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: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
14 OMIM references -
No MeSH references
No signs/symptoms info available.