You are using an outdated browser. Please upgrade your browser to improve your experience.

parkinsonian-pyramidal syndrome

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


GARD Rare
Mondo Description A Parkinson's disease that has material basis in mutation in the FBXO7 gene on chromosome 22q12.3.
Uniprot Description A neurodegenerative disorder characterized by parkinsonian and pyramidal signs. Clinical manifestations include tremor, bradykinesia, rigidity, postural instability, spasticity, mainly in the lower limbs, and hyperreflexia.
Disease Ontology Description A Parkinson's disease that has_material_basis_in mutation in the FBXO7 gene on chromosome 22q12.3.
Mondo Term and Equivalent IDs
MONDO:0009830:  parkinsonian-pyramidal syndrome
GARD:0009175: 
MESH:C538104: 
Orphanet:171695: 
UMLS:C1850100: