Human Gene Set: HP_PAROXYSMAL_DYSTONIA


Standard name HP_PAROXYSMAL_DYSTONIA
Systematic name M35744
Brief description Paroxysmal dystonia
Full description or abstract A form of dystonia characterized by episodes of dystonia (often hemidystonia or generalized) lasting from minutes to hours. There are no dystonic symptoms between episodes. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002268
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002268
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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