An instance of dystonic disorder that is caused by an inherited modification of the individual's genome. [ MONDO : patterns/hereditary ]

This is just here as a test because I lose it

Term information

database cross reference
  • OMIMPS:128100 (MONDO:equivalentTo)
  • UMLS:CN227322 (MONDO:equivalentTo)
  • Orphanet:391799 (MONDO:equivalentTo)
  • NCIT:C35527 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

definition
  • An instance of dystonic disorder that is caused by an inherited modification of the individual's genome.
exactMatch
  • http://www.orpha.net/ORDO/Orphanet_391799
  • http://purl.obolibrary.org/obo/NCIT_C35527
  • https://omim.org/phenotypicSeries/PS128100
  • http://linkedlifedata.com/resource/umls/id/CN227322
has exact synonym
  • hereditary dystonic disorder
  • rare genetic dystonia
  • rare genetic dystonic disorder
  • familial dystonia
id
  • MONDO:0044807
should conform to
  • http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml