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Parkinsonian-pyramidal syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal thrombocytopenia with normal platelets
3 OMIM references -
3 associated genes
No signs/symptoms info
Parkinsonian-pyramidal syndrome
Autosomal thrombocytopenia with normal platelets

FBXO7
(UniProt - OMIM)
 ANKRD26
(UniProt - OMIM)
SNCA
(UniProt - OMIM)
 CYCS
(UniProt - OMIM)
MASTL
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SNCA
(0.65)
CYCS


Citations in the biomedical literature:


Parkinsonian-pyramidal syndrome
FBXO7 SNCA
Autosomal thrombocytopenia with normal platelets
ANKRD26 CYCS MASTL



Parkinsonian-pyramidal syndrome
Autosomal thrombocytopenia with normal platelets

Synonym(s):
- Pallidopyramidal syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: -
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.