An instance of dystonic disorder that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]
Synonyms: hereditary dystonic disorder rare genetic dystonic disorder rare genetic dystonia familial dystonia
Term information
- UMLS:C5680022 (MONDO:equivalentTo)
- NANDO:1200511 (https://orcid.org/0000-0003-0011-764X)
- Orphanet:391799 (MONDO:equivalentTo)
- GARD:21630 (MONDO:GARD)
- NCIT:C35527 (MONDO:equivalentTo)
- MEDGEN:1842468 (MONDO:equivalentTo)
- OMIMPS:128100 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
http://www.orpha.net/ORDO/Orphanet_391799
http://purl.obolibrary.org/obo/NCIT_C35527
https://omim.org/phenotypicSeries/PS128100
http://identifiers.org/medgen/1842468
http://linkedlifedata.com/resource/umls/id/C5680022