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

Official abbreviation HMWKD
Name high molecular weight kininogen deficiency
OMIM ID 228960
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 15
Phenotype entries for this disease 15
Associated with 1 gene KNG1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2026-06-09 18:58:29 +02:00 (CEST)


Individuals

15 entries on 1 page. Showing entries 1 - 15.
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00412958 Pat5 PubMed: Barco 2020, Journal: Barco 2020 - F no Switzerland - - - - - HMWKD 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 - - - - - HMWKD Proband presenting with a prolonged aPTT KNG1 KNG1 1 3 Christian Drouet
00428672 - Journal: Nazir 2019 - F - Oman - - - - - HMWKD Proband presenting with a prolonged aPTT KNG1 KNG1 1 1 Christian Drouet
00428673 - Journal: Hayashi 1990 Undetectable plasma antigenic HK F likely Japan - - - - - HMWKD Proband presenting with a prolonged aPTT KNG1 KNG1 1 4 Christian Drouet
00428738 - Journal: Pancione 2013 Journal: Adenaeuer 2022 - M - Italy - - - - - HMWKD Homozygous proband presenting with a prolonged aPTT KNG1 - - 4 Christian Drouet
00428741 - Journal: Adenaeuer 2022 - F - Germany - - - - - HMWKD 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 - - - - - HMWKD 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 - - - - - HMWKD 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 - - - - - HMWKD Proband presenting with a markedly prolonged aPTT, with undetectable antigenic HK KNG1 KNG1 1 4 Christian Drouet
00430176 - PubMed: Ishimaru 1999 - F - Japan - - - - - HMWKD Homozygous proband presenting with a markedly prolonged aPTT KNG1 KNG1 1 1 Christian Drouet
00430224 - Journal: Yang 2020 - M yes China - - - - - HMWKD 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 - - - - - HMWKD Female homozygous proband presenting with a prolonged aPTT KNG1 KNG1 1 6 Christian Drouet
00453459 - Journal: Chen 2024 - F - China - - - - - HMWKD 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 - - - - - HMWKD Proband presenting with a significant prolongation of the APTT without any bleeding disorder KNG1 KNG1 2 1 Christian Drouet
00480023 patient PubMed: Huang 2026, Journal: Huang 2026 3-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M no China - - - - - HMWKD Proband presenting with an isolated, prolonged APTT without bleeding symptoms - identified during preoperative screening. KNG1 KNG1 2 1 Christian Drouet
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