Disease #00604 (WAD (dysostosis, acrodental, Weyers (WAD)), OMIM:193530)

Official abbreviation WAD
Name dysostosis, acrodental, Weyers (WAD)
OMIM ID 193530
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 2 genes EVC, EVC2
Associated tissues -
Disease features autosomal dominant
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

5 entries on 1 page. Showing entries 1 - 5.
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00325942 - PubMed: Ye 2006 5-generation famiy, 11 affected (6F, 5M) F - China Han Chinese - - - - WAD see paper; ... EVC2 EVC2 1 11 Johan den Dunnen
00326026 Pat21 PubMed: D'Asdia 2013 - M no United Kingdom (Great Britain) - - - - - WAD short stature, postaxial polydactyly, nail hypoplasia, teeth abnormalities EVC, EVC2 EVC2 1 1 Johan den Dunnen
00326083 Pat33 PubMed: Valencia 2009 4-generation family, 5 affected (3F, 2M) F;M no United Kingdom (Great Britain) - - - - - WAD - EVC, EVC2 EVC2 1 5 Johan den Dunnen
00326084 Pat26 PubMed: Valencia 2009 2-generation family, 1 affected, unaffected non-carrier parents - no Switzerland - - - - - WAD - EVC, EVC2 EVC2 1 1 Johan den Dunnen
00326085 Pat27 PubMed: Valencia 2009 3-generation family, 5 affected (F, 4M) F;M no Italy - - - - - WAD - EVC, EVC2 EVC2 1 5 Johan den Dunnen
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