Disease #00625 (DJO (dystonia, juvenile-onset (DJO)), OMIM:607371)

Official abbreviation DJO
Name dystonia, juvenile-onset (DJO)
OMIM ID 607371
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 1
Associated with 1 gene ACTB
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00132770 - - - - - Germany - - - - - DJO dystonia, myoclonic (DYT-11) SGCE SGCE 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00204319 - - - - - - - - - - - DJO - ACTB ACTB 1 1 SIB - Livia Famiglietti
00401304 062P - - F no Spain - - - - - BRWS1, DJO, ID - - ACTB 1 1 Alejandro Brea-Fernández
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