Disease #00463 (CDTB;CDB2 (dystrophy, corneal, Thiel-Behnke type (CDTB, corneal dystrophy of Bowman layer type2 (CDB-2))), OMIM:602082)

Official abbreviation CDTB;CDB2
Name dystrophy, corneal, Thiel-Behnke type (CDTB, corneal dystrophy of Bowman layer type2 (CDB-2))
OMIM ID 602082
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 4
Associated with 1 gene TGFBI
Associated tissues -
Disease features -
Remarks -
Date created 2014-07-21 14:36:45 +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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00019127 - PubMed: Chang et al .2009 - - - - China - - - - CDTB;CDB2 CDTB TGFBI TGFBI 1 1 Daniel Schorderet
00019175 - PubMed: Cho 2012, PubMed: El Ashry et al 2005, PubMed: Takacs 2007 - - - - Korea+British+France+Hungaria+Chinese+japan - - - - CDTB;CDB2 CDTB TGFBI TGFBI 1 1 Daniel Schorderet
00019176 - PubMed: Niel-Butschi 2011 - - - - France - - - - CDTB;CDB2 CDTB atypical TGFBI TGFBI 2 1 Daniel Schorderet
00019178 - PubMed: Zenteno 2009 - - - - Mexico - - - - CDRB;CDB1, CDTB;CDB2 CDRB ou TBCD TGFBI TGFBI 1 1 Daniel Schorderet
00319928 - - - - - (Morocco) - - - - - CDTB;CDB2 - TGFBI TGFBI 1 1 Yahya Benbouchta
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