Hemolytic anemia due to adenylate kinase deficiency 766982000
SNOMED CT code
SNOMED code | 766982000 |
---|---|
name | Hemolytic anemia due to adenylate kinase deficiency |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Hemolytic anemia due to adenylate kinase deficiency (disorder) |
synonyms |
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attributes - group3 | |
Has interpretation | Present 52101004 |
Interprets | Hemolysis 404227002 |
attributes - group2 | |
Interprets | Red blood cell count 14089001 |
Has interpretation | Below reference range 281300000 |
attributes - group5 | |
Finding site | Erythrocyte 41898006 |
attributes - group1 | |
Interprets | Measurement of total hemoglobin concentration 441689006 |
Has interpretation | Below reference range 281300000 |
attributes - group4 | |
Due to | Deficiency of adenylate kinase 124340003 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Red blood cell disorder 38292009 Hereditary red blood cell disorder 414394009 Hereditary hemolytic anemia 38911009 Hereditary nonspherocytic hemolytic anemia 301317008 Hemolytic anemia due to adenylate kinase deficiency 766982000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 Anemia 271737000 Anemia due to metabolic disorder 737220002 Anemia due to enzymopathy 351181000119103 Hemolytic anemia due to adenylate kinase deficiency 766982000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hemolytic anemia due to adenylate kinase deficiency 766982000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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