Disease #03927 (PNH2 (hemoglobinuria, nocturnal, paroxysmal, type 2 (PNH-2)), OMIM:615399)

Official abbreviation PNH2
Name hemoglobinuria, nocturnal, paroxysmal, type 2 (PNH-2)
OMIM ID 615399
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Somatic mutation
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PIGT
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

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00024929 - PubMed: Krawitz 2013, Journal: Krawitz 2013 - F no Germany - - - - - PNH2 see paper, detailed description PIGT PIGT 2 1 Johan den Dunnen
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