Disease #00179 (BDB1 (brachydactyly, type B1 (BDB1)), OMIM:113000)

Official abbreviation BDB1
Name brachydactyly, type B1 (BDB1)
OMIM ID 113000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 12
Phenotype entries for this disease 12
Associated with 1 gene ROR2
Associated tissues -
Disease features -
Remarks -
Date created 2013-08-28 18:20:45 +02:00 (CEST)
Date last edited 2020-09-29 10:08:02 +02:00 (CEST)


Individuals

12 entries on 1 page. Showing entries 1 - 12.
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00029686 - PubMed: Racacho 2015, Journal: Racacho 2015 - F no (Canada) white - - - - BDB1 see paper BMPR1B BMPR1B 1 1 Dennis E. Bulman
00311820 - PubMed: Oldridge 2000 3 patients from 3 families - - England - - - - - BDB1 - ROR2 ROR2 1 3 Jacopo Celli
00311821 - PubMed: Oldridge 2000 1 family, 3 patients - - Germany - - - - - BDB1 - ROR2 ROR2 1 3 Jacopo Celli
00311822 - PubMed: Oldridge 2000 1 family, 2 patients - - Portugal - - - - - BDB1 - ROR2 ROR2 1 2 Jacopo Celli
00311827 - PubMed: Schwabe 2000 1 family, 3 patients - - Germany - - - - - BDB1 - ROR2 ROR2 1 3 Jacopo Celli
00311828 - PubMed: Schwabe 2000 1 family, 10 patients (1 patient is homozygous) - - Turkey - - - - - BDB1 - ROR2 ROR2 1 10 Jacopo Celli
00311829 - PubMed: Schwabe 2000 2 families, 5 patients - - Germany - - - - - BDB1 - ROR2 ROR2 1 5 Jacopo Celli
00311830 - PubMed: Schwabe 2000 1 family, 1 patient - - Germany - - - - - BDB1 - ROR2 ROR2 1 1 Jacopo Celli
00311835 - PubMed: Bacchelli 2003 1 family, 3 patients; family originally described as HBND - - Wales - - - - - BDB1 - ROR2 ROR2 1 3 Jacopo Celli
00311836 - PubMed: Yang 2004 1 family, 1 patient - - China - - - - - BDB1 - ROR2 ROR2 1 1 Jacopo Celli
00311837 - PubMed: Hellani 2009 1 family, 1 patient - - Saudi Arabia - - - - - BDB1 - ROR2 ROR2 1 1 Jacopo Celli
00311841 - PubMed: Hamamy 2006 1 family, 2 patients - - Jordan - - - - - BDB1 - ROR2 ROR2 1 2 Jacopo Celli
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