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

disease_grouping, ordo_group_of_disorders

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml

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 dystonic disorder

rare genetic dystonia

familial dystonia

id

MONDO:0044807

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml