Disease #01212 (BDD (brachydactyly, type D (BD-D)), OMIM:113200)

Official abbreviation BDD
Name brachydactyly, type D (BD-D)
OMIM ID 113200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene HOXD13
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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00079982 - PubMed: Johnson 2003 4-generation family, 12 affecteds (only 9 individuals examined: 6F, 3M) F;M - (United Kingdom (Great Britain)) - - - - - BDD, BDE2 - HOXD13 HOXD13 1 12 Arrate Pereda
00079983 - PubMed: Johnson 2003 4-generation family, 8 affecteds (6F, 2M) F;M - (United Kingdom (Great Britain)) - - - - - BDD, BDE2 - HOXD13 HOXD13 1 8 Arrate Pereda
00079984 - PubMed: Johnson 2003 3-generation family, 8 affecteds (only 7 individuals examined 4F, 3M) F;M - (United Kingdom (Great Britain)) - - - - - BDD, BDE2 - HOXD13 HOXD13 1 8 Arrate Pereda
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