/parkinsonian-pyramidal syndrome

parkinsonian-pyramidal syndrome

Rare Disease

MONDO:0009830

Also Known As

Pallidopyramidal syndromeParkinson disease 15, autosomal recessiveautosomal recessive early-onset Parkinson disease 15autosomal recessive early-onset Parkinson disease type 15pallidopyramidal syndromeparkinsonian-pyramidal syndromePARK15Parkinson disease 15, autosomal recessive early-onsetautosomal recessive early-onset Parkinson's disease 15pallido-pyramidal diseasepallido-pyramidal syndrome

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

FBXO7 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

Related Diseases

paralysis agitans, juvenile, of Hunt

MONDO:0008193

Rare

late-onset Parkinson disease

MONDO:0008199

Rare

Parkinson disease, mitochondrial

MONDO:0010796

Parkinson disease 16

MONDO:0013167

young-onset Parkinson disease

MONDO:0017279

Rare

Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development

MONDO:0957576

← Back to All Diseases

parkinsonian-pyramidal syndrome

Also Known As

Definition

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases