Parkinsonian-pyramidal syndrome
Parkinson's disease that has material basis in mutation in the FBXO7 gene on chromosome 22q12.3
Press Enter · cited answer in seconds
0 sources
Summary
Parkinsonian-pyramidal syndrome is a rare disease[1].
Key Facts
- Parkinsonian-pyramidal syndrome's instance of is recorded as rare disease[2].
- Parkinsonian-pyramidal syndrome's instance of is recorded as class of disease[3].
- Parkinsonian-pyramidal syndrome's subclass of is recorded as young-onset Parkinson disease[4].
- Parkinsonian-pyramidal syndrome's subclass of is recorded as autosomal recessive disease[5].
- Parkinsonian-pyramidal syndrome's MeSH descriptor ID is recorded as C538104[6].
- Parkinsonian-pyramidal syndrome's OMIM ID is recorded as 260300[7].
- Parkinsonian-pyramidal syndrome's Disease Ontology ID is recorded as DOID:0060372[8].
- Parkinsonian-pyramidal syndrome's Orphanet ID is recorded as 171695[9].
- Parkinsonian-pyramidal syndrome's NCI Thesaurus ID is recorded as C198607[10].
- Parkinsonian-pyramidal syndrome's genetic association is recorded as FBXO7[11].
- Parkinsonian-pyramidal syndrome's genetic association is recorded as SNCA[12].
- Parkinsonian-pyramidal syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060372[13].
- Parkinsonian-pyramidal syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060372[14].
- Parkinsonian-pyramidal syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_171695[15].
- Parkinsonian-pyramidal syndrome's UMLS CUI is recorded as C1850100[16].
- Parkinsonian-pyramidal syndrome's ICD-10-CM is recorded as G20[17].
- Parkinsonian-pyramidal syndrome's GARD rare disease ID is recorded as 9175[18].
- Parkinsonian-pyramidal syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
- Parkinsonian-pyramidal syndrome's Mondo ID is recorded as MONDO_0009830[20].
- Parkinsonian-pyramidal syndrome's UniProt disease ID is recorded as DI-02139[21].