Disease #01716 (C1SD (complement component c1r/c1s deficiency (C1SD)), OMIM:216950)

Official abbreviation C1SD
Name complement component c1r/c1s deficiency (C1SD)
OMIM ID 216950
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 3
Associated with 1 gene C1R
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2015-12-08 23:59:30 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00418696 - Journal: Wu 2011 - M no United States - - - - - C1SD Proband presenting with a LES phenotype C1R - - 11 Christian Drouet
00435252 - Journal: Abe 2009 - F no Japan - - - - - C1SD Proband presenting with a complete C1s and C1r deficiency, developing seizure, fever, unilateral sacroileitis and ANA+ at age 16y C1S C1S 2 2 Christian Drouet
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