Disease #04232 (TMBTS (Temple-Baraitser syndrome (TMBTS)), OMIM:611816)

Official abbreviation TMBTS
Name Temple-Baraitser syndrome (TMBTS)
OMIM ID 611816
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 2
Associated with 1 gene KCNH1
Associated tissues -
Disease features -
Remarks -
Date created 2015-03-30 22:45:59 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00037515 - PubMed: Simons C 2015 - M no Australia - - - - - TMBTS - KCNH1 KCNH1 1 1 Philippe Campeau
00037516 - PubMed: Simons C 2015 - F no United States white - - - - TMBTS - KCNH1 KCNH1 1 1 Philippe Campeau
00037517 - PubMed: Simons C 2015 - M no Turkey - - - - - TMBTS - KCNH1 KCNH1 1 1 Philippe Campeau
00037518 - PubMed: Simons C 2015 - F no Algeria - - - - - TMBTS - KCNH1 KCNH1 1 1 Philippe Campeau
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