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Hereditary red blood cell disorder 414394009 SNOMED CT code SNOMED code 414394009 name Hereditary red blood cell disorder status active date introduced 2005-01-31 fully specified name(s) Hereditary red blood cell disorder (disorder) synonyms Hereditary red blood cell disorder attributes - group1 Finding site Erythrocyte 41898006 parents Red blood cell disorder 38292009 Hereditary disorder of cellular element of blood 414393003 children Adult-onset autosomal recessive sideroblastic anemia 720465002 Autosomal dominant secondary polycythemia 783202008 Autosomal recessive congenital methemoglobinemia 767497003 Congenital dyserythropoietic anemia 52951008 Congenital elliptocytosis 178935009 removed: 2020-01-31 Cystic fibrosis with gastritis and megaloblastic anemia syndrome 720401009 Dehydrated hereditary stomatocytosis 715526002 Familial erythrocytosis 17342003 Familial pseudohyperkalemia 717254007 Hereditary acanthocytosis 11376001 Hereditary hemoglobinopathy 427306008 Hereditary hemolytic anemia 38911009 Hereditary methemoglobinemia, enzymatic type 123768009 removed: 2018-07-31 Hereditary pyropoikilocytosis 9434008 Hereditary stomatocytosis 14087004 Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome 733064004 Overhydrated hereditary stomatocytosis 722125003 Phosphatidylcholine-sterol acyltransferase deficiency 49227001 removed: 2023-02-28 Primary CD59 deficiency 778027003 Southeast Asian ovalocytosis 723623002 Upshaw-Schulman syndrome 373420004 X chromosome-linked sideroblastic anemia 48983004 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 362965005 38292009 414394009 138875005 404684003 299691001 414022008 414393003 414394009 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
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