Paralysis agitans, juvenile, of hunt

Preferred Label : Paralysis agitans, juvenile, of hunt;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Parkinson disease, juvenile, of hunt;

Inheritance : Autosomal dominant;

Prefixed ID : 168100;

Details

Origin ID

168100;

UMLS CUI

C0238344;

Currated CISMeF NLP mapping
- Juvenile paralysis agitans of Hunt (disorder) [SNOMED CT concept]
- juvenile paralysis agitans of hunt [SNOMED Notion]
- paralysis agitans, juvenile, of hunt [MeSH concept]
- paralysis agitans, juvenile, of hunt [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bradykinesia [HPO term]
- Dysarthria [HPO term]
- Dystonia [HPO term]
- Gait disturbance [HPO term]
- Mask-like facies [HPO term]
- Parkinsonism [HPO term]
- Rigidity [HPO term]
- Slowly progressive [HPO term]
- Tremor [HPO term]
- Very slow progression [HPO term]
ORDO concept(s)
- Parkinsonian-pyramidal syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Juvenile paralysis agitans of Hunt (disorder) [SNOMED CT concept]
- juvenile paralysis agitans of hunt [SNOMED Notion]
- paralysis agitans, juvenile, of hunt [MeSH Supplementary Concept]
- paralysis agitans, juvenile, of hunt [MeSH concept]

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