Disease #00140 (HLHS2 (heart, hypoplastic left, syndrome, type 2 (HLHS-2)), OMIM:614435)

Official abbreviation HLHS2
Name heart, hypoplastic left, syndrome, type 2 (HLHS-2)
OMIM ID 614435
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene NKX2-5
Associated tissues -
Disease features -
Remarks -
Date created 2013-06-10 12:06:23 +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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00001385 - - Hypoplastic left heart syndrome with mitral atresia and aortic atresia. F - - African American - - - - CHD, HLHS2 - FOXP1 FOXP1 1 1 Vidu Garg
00170818 02529 - - F ? Italy white 47y - - - HLHS2 recurrent miscarriage, atrial fibrillation, atrial flutter, left ventricular noncompaction, Brugada syndrome DSG2, NKX2-5, TMEM43, TMEM45B DSG2, NKX2-5 2 1 Emanuele Micaglio
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