Disease #05849 (DYT28 (dystonia, type 28, childhood-onset (DYT28)), OMIM:617284)

Official abbreviation DYT28
Name dystonia, type 28, childhood-onset (DYT28)
OMIM ID 617284
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene KMT2B
Associated tissues -
Disease features -
Remarks -
Date created 2020-09-30 10:31:09 +02:00 (CEST)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00391790 171P - - M no Spain - - - - - DYT28 - - KMT2B 1 1 Alejandro Brea-Fernández
00398354 - - - M - - - - - - - DYT28 craniofacial dystonia (HP:0012179) KMT2B KMT2B 1 1 Bianca Rose Grosz
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