Parkinson disease 11, autosomal dominant, susceptibility to

Preferred Label : Parkinson disease 11, autosomal dominant, susceptibility to;

Symbol : PARK11;

CISMeF acronym : PARK11;

Type : Phenotype, molecular basis known;

Prefixed ID : #607688;

Détails

Origin ID

607688;

UMLS CUI

C4083045;

Broader ORDO disease(s)
- Young-onset Parkinson disease [ORDO Disease]
Currated CISMeF NLP mapping
- parkinson disease 11 [MeSH Supplementary Concept]
Genes related to phenotype
- Grb10-interacting gyf protein 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bradykinesia [HPO term]
- Parkinsonism with favorable response to dopaminergic medication [HPO term]
- Postural instability [HPO term]
- Resting tremor [HPO term]
- Rigidity [HPO term]
ORDO concept(s)
- Hereditary late-onset Parkinson disease [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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