Disease #03803 (CHTD2 (heart defects, congenital, nonsyndromic, type 2 (CHTD2), OMIM:614980)

Official abbreviation CHTD2
Name heart defects, congenital, nonsyndromic, type 2 (CHTD2
OMIM ID 614980
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene TAB2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-05-05 07:55:12 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00377278 P I8 - - F no (Switzerland) central european, white >05y - - - CHTD2 - TAB2 TAB2 1 1 Cecilia Giunta
00377280 P I9 - - F no Switzerland central european, white >13y - - - CHTD2 cardiovascular anomalies, recurrent facial dysmorphisms, generalized joint hypermobility and soft/velvetyhyperextensible skin TAB2 TAB2 1 1 Cecilia Giunta
00377296 - - - M no Belgium whitet - - - - CHTD2 cardiomyopathy,dilated aortic dissection type B inguinal hernia hypospadias multicystic kindney gastro-intestinal malrotation conductive hearing loss short stature facial dysmorphism (ptosis, hypotelorism) prostate cancer - TAB2 1 1 Jeroen Breckpot
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