Disease #00460 (CDGG1 (dystrophy, corneal, Groenouw type I (CDGG-1)), OMIM:121900)

Official abbreviation CDGG1
Name dystrophy, corneal, Groenouw type I (CDGG-1)
OMIM ID 121900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene TGFBI
Associated tissues -
Disease features -
Remarks -
Date created 2014-07-21 14:25:53 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00019123 - PubMed: Zenteno 2006 - - - - Mexico - - - - CDGG1 CDGGI TGFBI TGFBI 1 1 Daniel Schorderet
00019129 - PubMed: Stewart 1999b - - - - Asiatic - - - - CDGG1 CDGG1 TGFBI TGFBI 1 1 Daniel Schorderet
00019148 - PubMed: Paliwal 2010 - - - - India - - - - CDGG1 CDGG1 TGFBI TGFBI 1 1 Daniel Schorderet
00019166 - PubMed: Yu 2008 - - - - China - - - - CDGG1 CDGG1 atypical TGFBI TGFBI 1 1 Daniel Schorderet
00019177 - PubMed: Munier 1997, PubMed: El-Ashryr 2005 - - - - Mexico+ India+France+British+chinese+Japan+Turkish+Hungaria - - - - CDGG1 CDGG1 TGFBI TGFBI 1 1 Daniel Schorderet
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