Disease #03522 (HMOX1D (heme oxygenase 1 deficiency (HMOX1D)), OMIM:614034)

Official abbreviation HMOX1D
Name heme oxygenase 1 deficiency (HMOX1D)
OMIM ID 614034
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene HMOX1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2016-01-14 06:52:04 +01:00 (CET)


Individuals

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00057175 - {PMID:Yachie:1999:9884342} 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Japan - >06y - - regular transfusions of erythrocytes HMOX1D see paper; severe growth retardation, persistent hemolytic anemia characterized by marked erythrocyte fragmentation and intravascular hemolysis, with paradoxical increase serum haptoglobin and low bilirubin, abnormal coagulation/fibrinolysis system, associated with elevated thrombomodulin and von Willebrand factor, indicated severe, persistent endothelial damage; electron microscopy renal glomeruli revealed endothelium detachment, with subendothelial deposition of unidentified material; iron deposition renal/hepatic tissue, ... HMOX1 HMOX1 2 1 Johan den Dunnen
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