Disease #01185 (EA2 (ataxia, episodic, type 2), OMIM:108500)

Official abbreviation EA2
Name ataxia, episodic, type 2
OMIM ID 108500
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 9
Phenotype entries for this disease 4
Associated with 1 gene CACNA1A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-03-22 16:51:15 +01:00 (CET)


Individuals

9 entries on 1 page. Showing entries 1 - 9.
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00110588 - - - - - (Germany) - - - - - EA2 - CACNA1A CACNA1A 1 1 Birgit Neitzel
00110605 - - - - - (Germany) - - - - - EA2 - CACNA1A CACNA1A 3 1 Birgit Neitzel
00110614 - - - - - (Germany) - - - - - EA2 episodic atxia CACNA1A CACNA1A 2 1 Birgit Neitzel
00110645 - - - - - (Germany) - - - - - EA2 episodic atxia CACNA1A CACNA1A 1 1 Birgit Neitzel
00110661 - - - - - (Germany) - - - - - EA2 - CACNA1A CACNA1A 1 1 Birgit Neitzel
00110683 - - - - - (Germany) - - - - - EA2 - CACNA1A CACNA1A 1 1 Birgit Neitzel
00234405 - - - - - - - - - - - EA2 - CACNA1A CACNA1A 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00332980 175852 - - M ? Germany - - - - - EA2 (+) Ataxia,(+) Vertigo,(+) Abnormality of coordination CACNA1A CACNA1A 1 1 Andreas Laner
00452065 287499 - - F no Germany - - - - - EA2 Gait disturbance, Vertigo, Iron deficiency anemia, Ataxia, episodic, family history (father and brother) CACNA1A CACNA1A 1 1 Andreas Laner
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