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Hereditary persistence of fetal hemoglobin thalassemia 16964007 SNOMED CT code SNOMED code 16964007 name Hereditary persistence of fetal hemoglobin thalassemia status active date introduced 2002-01-31 fully specified name(s) Hereditary persistence of fetal hemoglobin thalassemia (disorder) synonyms Hereditary persistence of foetal haemoglobin thalassaemia Hereditary persistence of fetal hemoglobin thalassemia Hereditary persistence of fetal haemoglobin thalassaemia HPFH (hereditary persistence of fetal haemoglobin) beta-thalassaemia syndrome HPFH (hereditary persistence of fetal hemoglobin) beta-thalassemia syndrome attributes - group2 Interprets Measurement of total hemoglobin concentration 441689006 Has interpretation Below reference range 281300000 attributes - group3 Occurrence Congenital 255399007 Finding site Erythrocyte 41898006 parents Thalassemia 40108008 children Hereditary persistence of fetal hemoglobin delta beta plus thalassemia 54006005 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia 61395005 HPFH A gamma beta^+^ thalassemia 39586009 HPFH deletion type 85557000 HPFH linked to beta-globulin gene cluster 89459006 HPFH nondeletion type 56205004 HPFH unlinked to beta-globulin gene cluster 32855007 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 66091009 427306008 40108008 16964007 ancestors sorted most to least specific
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