Phenotypes for disease #03522 (HMOX1D (heme oxygenase 1 deficiency (HMOX1D)), OMIM:614034)

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AscendingPhenotype ID     

Phenotype details     

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Age/Diagnosis     

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Individual ID     
0000043860 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, ... - - Familial, autosomal recessive - - 02y02m recurrent fever (HP:0001954), generalized erythematous rash (HP:0007432) - Johan den Dunnen 00057175
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