Parkinson-dementia syndrome

Preferred Label : Parkinson-dementia syndrome;

Type : Phenotype, molecular basis known;

Included titles and symbols : Supranuclear palsy, progressive, 1, atypical; Steele-richardson-olszewski syndrome, atypical;

Inheritance : Autosomal recessive vs. dominant with low penetrance and expression;

Prefixed ID : #260540;

Détails

Origin ID

260540;

UMLS CUI

C1850077;

Automatic exact mappings (from CISMeF team)
- Atypical progressive supranuclear palsy syndrome [ORDO Disease]
- Progressive supranuclear palsy-parkinsonism syndrome [ORDO Disease]
- progressive supranuclear palsy atypical [MeSH Supplementary Concept]
Genes related to phenotype
- Microtubule-associated protein tau [OMIM gene]
HPO term(s)
- Abnormal pyramidal sign [HPO term]
- Adult onset [HPO term]
- Autosomal recessive inheritance [HPO term]
- Dementia [HPO term]
- Kyphoscoliosis [HPO term]
- Morphological abnormality of the pyramidal tract [HPO term]
- Ophthalmoparesis [HPO term]
- Parkinsonism [HPO term]
- Rigidity [HPO term]
- Tremor [HPO term]
- Young adult onset [HPO term]
ORDO concept(s)
- Atypical progressive supranuclear palsy syndrome [ORDO Disease]
- Progressive supranuclear palsy [ORDO Disease]
- Progressive supranuclear palsy-parkinsonism syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atypical progressive supranuclear palsy syndrome [ORDO Disease]
- Progressive supranuclear palsy atypical [MeSH concept]
- progressive supranuclear palsy atypical [MeSH Supplementary Concept]

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

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