Disease #00462 (CDA (dystrophy, cornea, Avellino type (CDA)), OMIM:607541)

Official abbreviation CDA
Name dystrophy, cornea, Avellino type (CDA)
OMIM ID 607541
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 8
Phenotype entries for this disease 8
Associated with 1 gene TGFBI
Associated tissues -
Disease features -
Remarks -
Date created 2014-07-21 14:34:39 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00019126 - PubMed: Edelstein 2010 - - - - Unknown (white male) - - - - CDA CDA TGFBI TGFBI 1 1 Daniel Schorderet
00019130 - PubMed: Munier 1997 - - - - Japan / Europa / white / Korea/ Britany/ Germany/ Spain/ China/ Afro-american - - - - CDA CDA TGFBI TGFBI 1 1 Daniel Schorderet
00019131 - PubMed: Mashima 1997, PubMed: Cho 2012 - - - - Japan/ indo-parkistan/ north china/ Iranian - - - - CDA CDA (resseembling SVGD) TGFBI TGFBI 1 1 Daniel Schorderet
00019133 - PubMed: Watanabe et al.2001 - - - - Japan (Tottori) - - - - CDA CDA (type II corneal opacity: reticular) TGFBI TGFBI 1 1 Daniel Schorderet
00019134 - PubMed: Yamada et al.2009 - - - - Japan - - - - CDA CDL+CDA TGFBI TGFBI 2 1 Daniel Schorderet
00019135 - PubMed: Yam 2012 - - - - China - - - - CDA CDA (with no lattice-type deposition observed) TGFBI TGFBI 2 1 Daniel Schorderet
00019172 - PubMed: Zenteno 2009 - - - - Mexico - - - - CDA CDA TGFBI TGFBI 1 1 Daniel Schorderet
00073732 - Journal: Fatkin 2016 - F - - - - - - - CDA LVEF 0.36, skeletal myopathy (HP:0003756), implantable cardioverter-defibrillator DES DES 2 1 Johan den Dunnen
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