Term info
database cross reference
- NCIT:C35527 (MONDO:equivalentTo)
- UMLS:CN227322 (MONDO:equivalentTo)
- OMIMPS:128100 (MONDO:equivalentTo)
- Orphanet:391799 (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
https://omim.org/phenotypicSeries/PS128100, http://purl.obolibrary.org/obo/NCIT_C35527, http://linkedlifedata.com/resource/umls/id/CN227322, http://purl.obolibrary.org/obo/Orphanet_391799
has exact synonym
hereditary dystonic disorder, rare genetic dystonia, rare genetic dystonic disorder, familial dystonia
id
MONDO:0044807