Phenotype Library | Search Phenotypes

Parkinsonian-Pyramidal Syndrome (MONDO:0009830)

A Parkinson's disease that has material basis in mutation in the FBXO7 gene on chromosome 22q12.3.

Overview

Category

Ontology ID

Internal:11034

Synonyms

Pallidopyramidal syndrome

Parkinson disease 15, autosomal recessive

autosomal recessive early-onset Parkinson disease type 15

pallidopyramidal syndrome

parkinsonian-pyramidal syndrome

PARK15

Parkinson disease 15, autosomal recessive early-onset

autosomal recessive early-onset Parkinson's disease 15

pallido-pyramidal disease

pallido-pyramidal syndrome

Mapped terms

DOID:0060372

GARD:0009175

MEDGEN:337969

MESH:C538104

OMIM:260300

Orphanet:171695

UMLS:C1850100

icd11.foundation:1128311778

Child terms