Disease #02726 (SPENCDI (Spondyloenchondrodysplasia, with immune dysregulation (SPENCDI)), OMIM:607944)

Official abbreviation SPENCDI
Name Spondyloenchondrodysplasia, with immune dysregulation (SPENCDI)
OMIM ID 607944
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 10
Phenotype entries for this disease 10
Associated with 1 gene ACP5
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

10 entries on 1 page. Showing entries 1 - 10.
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00117855 - PubMed: Briggs 2011 - F - France - - - - - SPENCDI - ACP5 ACP5 1 1 Marcin Szynkiewicz
00117856 - PubMed: Briggs 2011 consanguineous parents (uncle-niece) M yes India - - - - - SPENCDI - ACP5 ACP5 1 1 Marcin Szynkiewicz
00117857 - PubMed: Briggs 2011 brother patient 5; consanguineous parents (first cousins) M yes Turkey - - - - - SPENCDI - ACP5 ACP5 1 1 Marcin Szynkiewicz
00117858 - PubMed: Briggs 2011 sister patient 4; consanguineous parents (first cousins) F yes Turkey - - - - - SPENCDI - ACP5 ACP5 1 1 Marcin Szynkiewicz
00117859 - PubMed: Briggs 2011 twin sister patient 3 - - Austria - - - - - SPENCDI - ACP5 ACP5 2 1 Marcin Szynkiewicz
00117860 - PubMed: Briggs 2011 twin brother patient 2 M - Austria - - - - - SPENCDI - ACP5 ACP5 2 1 Marcin Szynkiewicz
00117861 - PubMed: Briggs 2011 - F - Mali - - - - - SPENCDI - ACP5 ACP5 1 1 Marcin Szynkiewicz
00117862 - PubMed: Briggs 2011 consanguineous parents (first cousins) M yes Pakistan - - - - - SPENCDI - ACP5 ACP5 1 1 Marcin Szynkiewicz
00117863 - PubMed: Briggs 2011 - F - Egypt - - - - - SPENCDI - ACP5 ACP5 1 1 Marcin Szynkiewicz
00117864 - PubMed: Briggs 2011 consanguineous parents (first cousins) F yes Portugal - - - - - SPENCDI - ACP5 ACP5 1 1 Marcin Szynkiewicz
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