Disease #00369 (DYT1 (dystonia, torsion, early onset, type 1 (DYT-1)), OMIM:128100)

Official abbreviation DYT1
Name dystonia, torsion, early onset, type 1 (DYT-1)
OMIM ID 128100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene TOR1A
Associated tissues -
Disease features -
Remarks -
Date created 2014-04-15 16:59:03 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00016414 - PubMed: Ozelius 1997 patients from several different families - - - - - - - - DYT1 highly variable phenotype, reduced penetrance TOR1A TOR1A 1 4 Johan den Dunnen
00016415 - PubMed: Zirn 2008 2-generation family, unaffected carrier mother (reduced penetrance) F no Germany - >18y - - - DYT1 see paper TOR1A TOR1A 1 2 Johan den Dunnen
00016417 - PubMed: Lueng 2001 - M no Puerto Rico - - - - - DYT1 see paper TOR1A TOR1A 1 1 Johan den Dunnen
00016418 - PubMed: Lueng 2001, PubMed: Klein 2002, PubMed: Doheny 2002 3-generation, 4 affected carriers (2M, 2F), variable phenotype, SGCE:c.587T>G variant as well F no Italy;Lithuania;Poland - - - - - DYT1 see paper TOR1A TOR1A 1 4 Johan den Dunnen
00016420 - PubMed: Calakos 2010 - M - United States - - - - - DYT1 see paper, late-onset focal torsion dystonia TOR1A TOR1A 1 1 Johan den Dunnen
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