Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development

Preferred Label : Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development;

Symbol : PARK25;

Type : Phenotype, molecular basis known;

Prefixed ID : #620482;

Details

Origin ID

620482;

UMLS CUI

C5882680;

DO Cross reference
- Parkinson's disease 25 [DO Concept]
Genes related to phenotype
- Protein phosphatase 2 phosphatase activator [OMIM gene]
HPO term(s)
- Anxiety [HPO term]
- Autosomal recessive inheritance [HPO term]
- Bradykinesia [HPO term]
- Depression [HPO term]
- Disinhibition [HPO term]
- Drooling [HPO term]
- Intellectual disability [HPO term]
- Juvenile onset [HPO term]
- Parkinsonism with favorable response to dopaminergic medication [HPO term]
- Resting tremor [HPO term]
- Restless legs [HPO term]
- Rigidity [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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