Cytoscape Web
Click node...

Parkinsonian-pyramidal syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
1 OMIM reference -
1 associated gene
No signs/symptoms info
Parkinsonian-pyramidal syndrome
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

FBXO7
(UniProt - OMIM)
 DYNC1H1
(UniProt - OMIM)
SNCA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SNCA
(0.49)
DYNC1H1


Citations in the biomedical literature:


Parkinsonian-pyramidal syndrome
FBXO7 SNCA
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
DYNC1H1



Parkinsonian-pyramidal syndrome
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures

Synonym(s):
- Pallidopyramidal syndrome
Synonym(s):
- Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy without contractures
- SMALED1
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: unknown
Average age onset: childhood
Average age of death: adult
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.