Disease #03191 (ASD5 (septal defect, atrial, type 5 (ASD5)), OMIM:612794)

Official abbreviation ASD5
Name septal defect, atrial, type 5 (ASD5)
OMIM ID 612794
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ACTC1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00033835 - - 5-generation family 16 affecteds - - Sweden - - - - - ASD5 - ACTC1 ACTC1 1 16 Johan den Dunnen
00033836 - - 5-generation family 12 affecteds - - Sweden - - - - - ASD5 - ACTC1 ACTC1 1 12 Johan den Dunnen
00033837 - - - - - Sweden - - - - - ASD5 - ACTC1 ACTC1 1 2 Johan den Dunnen
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