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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:focal dystonia
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Accession:DOID:0050836 term browser browse the term
Definition:A dystonia that is localized to a specific part of the body. (DO)
Synonyms:exact_synonym: FTSD;   Musician's Dystonia;   focal dystonia, task-specific;   focal dystonias;   occupational cramp;   occupational dystonia;   task-specific dystonia
 primary_id: MESH:C566973
 alt_id: MIM:611284
 xref: GARD:6458

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show annotations for term's descendants           Sort by:
focal dystonia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Tor1a torsin family 1 member A ISO MouseDO NCBI chrNW_004624760:5,602,011...5,606,784
Ensembl chrNW_004624760:5,601,943...5,606,162 		JBrowse link
Benign Essential Blepharospasm term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Drd5 dopamine receptor D5 susceptibility ISO ClinVar Annotator: match by term: DRD5-related condition OMIM
ClinVar		 PMID:25741868 NCBI chrNW_004624755:21,358,586...21,361,410 JBrowse link
G Slc2a9 solute carrier family 2 member 9 ISO ClinVar Annotator: match by term: DRD5-related condition ClinVar PMID:25741868 NCBI chrNW_004624755:21,165,374...21,328,843
Ensembl chrNW_004624755:21,171,274...21,322,543 		JBrowse link
blepharospasm term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Drd5 dopamine receptor D5 ISO DNA:repeat
CTD Direct Evidence: marker/mechanism		 RGD
CTD		 PMID:11781417 RGD:734899 NCBI chrNW_004624755:21,358,586...21,361,410 JBrowse link
cervical dystonia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Actl6a actin like 6A ISO ClinVar Annotator: match by term: Torticollis ClinVar PMID:19215055 PMID:25741868 PMID:28649782 PMID:31994175 NCBI chrNW_004624730:57,305,105...57,337,653
Ensembl chrNW_004624730:57,305,053...57,337,797 		JBrowse link
G Arid1b AT-rich interaction domain 1B ISO ClinVar Annotator: match by term: Torticollis ClinVar PMID:25741868 NCBI chrNW_004624785:970,169...1,417,847
Ensembl chrNW_004624785:973,003...1,417,853 		JBrowse link
G Drd5 dopamine receptor D5 ISO CTD Direct Evidence: marker/mechanism CTD PMID:11459908 NCBI chrNW_004624755:21,358,586...21,361,410 JBrowse link
G LOC101703821 HLA class II histocompatibility antigen, DQ beta 1 chain ISO DNA:polymorphism (human) RGD PMID:20843162 RGD:5147570 NCBI chrNW_004624754:23,895,509...23,902,487
Ensembl chrNW_004624754:23,895,607...23,906,713 		JBrowse link
dystonia 23 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cacna1b calcium voltage-gated channel subunit alpha1 B ISO ClinVar Annotator: match by term: Dystonia 23 ClinVar PMID:21370267 PMID:25296916 PMID:25741868 PMID:26157024 PMID:28492532 NCBI chrNW_004624760:78,754...257,901
Ensembl chrNW_004624760:81,236...257,787 		JBrowse link
G Ciz1 CDKN1A interacting zinc finger protein 1 ISO ClinVar Annotator: match by term: Dystonia 23 ClinVar PMID:25741868 NCBI chrNW_004624760:6,653,710...6,672,357
Ensembl chrNW_004624760:6,654,659...6,672,237 		JBrowse link
dystonia 24 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ano3 anoctamin 3 ISO ClinVar Annotator: match by term: Dystonia 24 OMIM
ClinVar		 PMID:11009204 PMID:23200863 PMID:25741868 PMID:27666935 PMID:28492532 More... NCBI chrNW_004624766:16,340,636...16,605,724
Ensembl chrNW_004624766:16,340,630...16,605,724 		JBrowse link
oculogyric crisis term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atp1a3 ATPase Na+/K+ transporting subunit alpha 3 ISO ClinVar Annotator: match by term: Oculogyric crisis ClinVar PMID:15260953 PMID:20301294 PMID:21911500 PMID:22842232 PMID:22850527 More... NCBI chrNW_004624907:715,109...736,040
Ensembl chrNW_004624907:715,094...736,432 		JBrowse link
Parkinson's disease 15 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Fbxo7 F-box protein 7 ISO ClinVar Annotator: match by term: Parkinsonian-pyramidal syndrome OMIM
ClinVar		 PMID:9536098 PMID:16199547 PMID:17576681 PMID:18513678 PMID:19038853 More... NCBI chrNW_004624750:1,977,666...1,997,408
Ensembl chrNW_004624750:1,977,761...1,997,231 		JBrowse link
G Nf1 neurofibromin 1 ISO ClinVar Annotator: match by term: Parkinson disease 15 ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624875:3,636,762...3,959,991
Ensembl chrNW_004624875:3,636,924...3,956,576 		JBrowse link
torsion dystonia 7 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ciz1 CDKN1A interacting zinc finger protein 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:22447717 NCBI chrNW_004624760:6,653,710...6,672,357
Ensembl chrNW_004624760:6,654,659...6,672,237 		JBrowse link
X-linked dystonia-parkinsonism term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Taf1 TATA-box binding protein associated factor 1 ISO ClinVar Annotator: match by term: TAF1-related condition | ClinVar Annotator: match by term: X-linked dystonia-parkinsonism OMIM
ClinVar		 PMID:17273961 PMID:25741868 PMID:28492532 PMID:32396742 NCBI chrNW_004624903:1,698,201...1,774,607 JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14229
    disease of anatomical entity 13931
      nervous system disease 12269
        Neurologic Manifestations 9171
          Dyskinesias 2035
            dystonia 473
              focal dystonia 13
                X-linked dystonia-parkinsonism 1
                anismus 0
                blepharospasm + 4
                cervical dystonia + 4
                cranio-facial dystonia + 0
                dystonia 23 2
                dystonia 24 1
                focal hand dystonia 0
                oculogyric crisis 1
                oromandibular dystonia 0
                spasmodic dystonia 0
                torsion dystonia 7 1
Path 2
Term Annotations click to browse term
  disease 14229
    disease of anatomical entity 13931
      nervous system disease 12269
        central nervous system disease 10992
          brain disease 10306
            movement disease 2382
              Dyskinesias 2035
                dystonia 473
                  focal dystonia 13
                    X-linked dystonia-parkinsonism 1
                    anismus 0
                    blepharospasm + 4
                    cervical dystonia + 4
                    cranio-facial dystonia + 0
                    dystonia 23 2
                    dystonia 24 1
                    focal hand dystonia 0
                    oculogyric crisis 1
                    oromandibular dystonia 0
                    spasmodic dystonia 0
                    torsion dystonia 7 1
paths to the root