Disease #03601 (CIAT (cognitive impairment, ataxia, cerebellar (CIAT)), OMIM:614306)

Official abbreviation CIAT
Name cognitive impairment, ataxia, cerebellar (CIAT)
OMIM ID 614306
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene SCN8A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2019-10-25 11:02:39 +02:00 (CEST)


Individuals

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00149455 - - - - - Italy white 69y - - - AD, CIAT, FTD - GRN GRN 1 3 Marc Cruts
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