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Congenital anemia 63565007 SNOMED CT code SNOMED code 63565007 name Congenital anemia status active date introduced 2002-01-31 fully specified name(s) Congenital anemia (disorder) synonyms Congenital anemia Congenital anaemia attributes - group3 Occurrence Congenital 255399007 attributes - group1 Has interpretation Below reference range 281300000 Interprets Measurement of total hemoglobin concentration 441689006 attributes - group2 Has interpretation Below reference range 281300000 Interprets Red blood cell count 14089001 parents children [X]Other congenital anemias, not elsewhere classified 206670007 removed: 2009-01-31 Alpha plus thalassemia deletion type 86242003 Alpha plus thalassemia non deletion type 85422000 Alpha thalassemia X-linked intellectual disability syndrome 715342005 Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 734349003 Congenital anemia from fetal blood loss 206519009 removed: 2014-07-31 Congenital dyserythropoietic anemia 52951008 Congenital hemolytic anemia 42601008 Congenital hemolytic uremic syndrome 444976001 Congenital hypoplastic anemia 88854002 Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome 765327005 Congenital transferrin deficiency 234353009 Constitutional aplastic anemia 28975000 Epsilon gamma delta beta^0^ thalassemia 73190000 Gamma delta beta thalassemia 788944005 Ghosal hematodiaphyseal dysplasia 389214003 Hemoglobin Bart's hydrops syndrome 5300004 HNSHA due to hexokinase deficiency 42484009 HNSHA due to NADH diaphorase deficiency 47526003 HNSHA due to NADH-methemoglobin reductase deficiency 70517008 removed: 2018-07-31 Late anemia of newborn 276579007 Lethal hemolytic anemia and genital anomaly syndrome 719402008 Megaloblastic anemia due to inborn errors of metabolism 34925000 Physiological anemia of infancy 276578004 Severe combined immunodeficiency with reticular dysgenesis 190996002 Thalassemia in mother complicating childbirth 10806241000119108 Thalassemia in mother complicating pregnancy 72331000119105 Unstable hemoglobin disease 18273004 X chromosome-linked sideroblastic anemia 48983004 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 127325009 441742003 106200001 250220000 441793007 165397008 63565007 138875005 404684003 127325009 441742003 118245000 365625004 165427000 165423001 63565007 138875005 404684003 299691001 414022008 271737000 63565007 138875005 404684003 64572001 66091009 63565007 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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