Disease #01787 (high molecular weight kininogen deficiency, OMIM:228960)

Official abbreviation -
Name high molecular weight kininogen deficiency
OMIM ID 228960
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 14
Phenotype entries for this disease 14
Associated with 1 gene KNG1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-07-07 09:16:38 +02:00 (CEST)


Individuals

14 entries on 1 page. Showing entries 1 - 14.
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00412958 Pat5 PubMed: Barco 2020, Journal: Barco 2020 - F no Switzerland - - - - - high molecular weight kininogen deficiency Compound heterozygous female proband presenting with a prolonged aPTT with a low antigenic HK and LK KNG1 KNG1 2 1 Christian Drouet
00428671 - Journal: Adenaeuer 2023 - - - Italy - - - - - high molecular weight kininogen deficiency Proband presenting with a prolonged aPTT KNG1 KNG1 1 3 Christian Drouet
00428672 - Journal: Nazir 2019 - F - Oman - - - - - high molecular weight kininogen deficiency Proband presenting with a prolonged aPTT KNG1 KNG1 1 1 Christian Drouet
00428673 - Journal: Hayashi 1990 Undetectable plasma antigenic HK F likely Japan - - - - - high molecular weight kininogen deficiency Proband presenting with a prolonged aPTT KNG1 KNG1 1 4 Christian Drouet
00428738 - Journal: Pancione 2013 Journal: Adenaeuer 2022 - M - Italy - - - - - high molecular weight kininogen deficiency Homozygous proband presenting with a prolonged aPTT KNG1 - - 4 Christian Drouet
00428741 - Journal: Adenaeuer 2022 - F - Germany - - - - - high molecular weight kininogen deficiency Compound heterozygous proband presenting with a prolonged aPTT KNG1 KNG1 2 3 Christian Drouet
00430150 - Journal: Fukushima 2022 Homozygous proband with his three heterozygous children M - Japan - - - - - high molecular weight kininogen deficiency Proband presenting with a prolonged aPTT, with a strongly reduced expression of HK and LK KNG1 KNG1 1 4 Christian Drouet
00430159 - Journal: Jeung 2020 - M - Korea - - - - - high molecular weight kininogen deficiency Compound heterozygous proband presenting with prolonged aPTT, with undectectable functional an antigenic HK KNG1 KNG1 2 1 Christian Drouet
00430175 - Journal: Krijanovski 2003 Proband homozygous carrier presenting with a markedly prolonged APTT with a normal prothrombin time, thrombin time, and clottable fibrinogen. No antigenic HK detected M yes France - - - - - high molecular weight kininogen deficiency Proband presenting with a markedly prolonged aPTT, with undetectable antigenic HK KNG1 KNG1 1 4 Christian Drouet
00430176 - PubMed: Ishimaru 1999 - F - Japan - - - - - high molecular weight kininogen deficiency Homozygous proband presenting with a markedly prolonged aPTT KNG1 KNG1 1 1 Christian Drouet
00430224 - Journal: Yang 2020 - M yes China - - - - - high molecular weight kininogen deficiency Male homozygous proband and homozygous sisters presenting with a prolonged aPTT, with an absence of HK expression KNG1 KNG1 1 7 Christian Drouet
00430225 - Journal: Shigekiyo 2007 - F yes Japan - - - - - high molecular weight kininogen deficiency Female homozygous proband presenting with a prolonged aPTT KNG1 KNG1 1 6 Christian Drouet
00453459 - Journal: Chen 2024 - F - China - - - - - high molecular weight kininogen deficiency Proband presenting with a prolonged aPTT KNG1 KNG1 1 6 Christian Drouet
00460181 - Journal: Lv 2025 Single family with a compound heterozygous affected individual F no China - - - - - high molecular weight kininogen deficiency Proband presenting with a significant prolongation of the APTT without any bleeding disorder KNG1 KNG1 2 1 Christian Drouet
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