Disease #02825 (PPCD3 (dystrophy, corneal, posterior polymorphous, type 3 (PPCD-3)), OMIM:609141)

Official abbreviation PPCD3
Name dystrophy, corneal, posterior polymorphous, type 3 (PPCD-3)
OMIM ID 609141
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ZEB1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00046902 FamC17PatIII1 PubMed: Liskova 2016, Journal: Liskova 2016 4-generation family, 3 affected (3F, M), unaffected heterozygous carrier parents/relatives M no Czech Republic - - - - - PPCD3 diagnosed with posterior polymorphous corneal dystrophy 3 - ZEB1 1 4 Cerys Evans
00046903 FamC27 PubMed: Liskova 2016, Journal: Liskova 2016 - F ? Czech Republic - - - - - PPCD3 diagnosed with posterior polymorphous corneal dystropy 3 - ZEB1 1 1 Cerys Evans
00046952 PatB8 PubMed: Liskova 2016, Journal: Liskova 2016 - M ? United Kingdom (Great Britain) - - - - - PPCD3 - ZEB1 ZEB1 1 1 Cerys Evans
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