Disease #04389 (DYT23 (dystonia?, type 23 (DYT-23)), OMIM:614860)

Official abbreviation DYT23
Name dystonia?, type 23 (DYT-23)
OMIM ID 614860
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CACNA1B
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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