Parkinson disease 13, autosomal dominant, susceptibility to

Preferred Label : Parkinson disease 13, autosomal dominant, susceptibility to;

Symbol : PARK13;

CISMeF acronym : PARK13;

Type : Phenotype, molecular basis known;

Prefixed ID : #610297;

Details

Origin ID

610297;

UMLS CUI

C1853202;

Automatic exact mappings (from CISMeF team)
- HtrA serine peptidase 2 [ORDO Gene]
- HtrA serine peptidase 2 [HGNC gene]
Broader ORDO disease(s)
- Young-onset Parkinson disease [ORDO Disease]
Currated CISMeF NLP mapping
- parkinson disease 13 [MeSH Supplementary Concept]
Genes related to phenotype
- Htra serine peptidase 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bradykinesia [HPO term]
- Parkinsonism with favorable response to dopaminergic medication [HPO term]
- Rigidity [HPO term]
- Tremor [HPO term]
ORDO concept(s)
- Young-onset Parkinson disease [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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