Disease #05035 (SCA21 (ataxia, spinocerebellar, type 21 (SCA-21)), OMIM:607454)

Official abbreviation SCA21
Name ataxia, spinocerebellar, type 21 (SCA-21)
OMIM ID 607454
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene TMEM240
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00164324 P09182 - - M no Israel Jewish-Ashkenazi - - - - SCA21 - - SCYL1 1 2 Lior Cohen
00363500 178612 - - M ? Germany - - - - - SCA21 (+) Muscular hypotonia,(+) Motor delay,(+) Joint hypermobility,(+) Quadriceps muscle weakness,(+) Chronic constipation TMEM240 TMEM240 1 1 Andreas Laner
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