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Parkinsonian-pyramidal syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant Charcot-Marie-Tooth disease type 2L
1 OMIM reference -
1 associated gene
No signs/symptoms info
Parkinsonian-pyramidal syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2L

FBXO7
(UniProt - OMIM)
 HSPB8
(UniProt - OMIM)
SNCA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SNCA
(0.56)
HSPB8


Citations in the biomedical literature:


Parkinsonian-pyramidal syndrome
FBXO7 SNCA
Autosomal dominant Charcot-Marie-Tooth disease type 2L
HSPB8



Parkinsonian-pyramidal syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2L

Synonym(s):
- Pallidopyramidal syndrome
Synonym(s):
- CMT2L
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: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.