Disease #03263 (AT3D (antithrombin III deficiency (AT3D)), OMIM:613118)

Official abbreviation AT3D
Name antithrombin III deficiency (AT3D)
OMIM ID 613118
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene SERPINC1
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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00087227 - - - F no (Russian Federation) white - - - - AT3D - SERPINC1 SERPINC1 1 1 Yulia Rogozhina
00208839 - - - - - - - - - - - AT3D - SERPINC1 SERPINC1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00431009 - Journal: Mulder 2017 A British family with 2 affected individuals M no United Kingdom (Great Britain) - - - - - AT3D Proband presenting with thrombophilic disorders SERPINC1 SERPINC1 1 2 Christian Drouet
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