X chromosome-linked sideroblastic anemia 48983004
SNOMED CT code
SNOMED code | 48983004 |
---|---|
name | X chromosome-linked sideroblastic anemia |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | X chromosome-linked sideroblastic anemia (disorder) |
synonyms |
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attributes - group2 | |
Interprets | Red blood cell count 14089001 |
Has interpretation | Below reference range 281300000 |
attributes - group1 | |
Interprets | Measurement of total hemoglobin concentration 441689006 |
Has interpretation | Below reference range 281300000 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Finding site | Erythrocyte 41898006 |
parents |
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children | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 X chromosome-linked sideroblastic anemia 48983004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of porphyrin metabolism 29094004 Inherited disorder of porphyrin metabolism 403832004 X chromosome-linked sideroblastic anemia 48983004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Red blood cell disorder 38292009 Hereditary red blood cell disorder 414394009 X chromosome-linked sideroblastic anemia 48983004 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 Anemia 271737000 Sideroblastic anemia 41841004 X chromosome-linked sideroblastic anemia 48983004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital anemia 63565007 X chromosome-linked sideroblastic anemia 48983004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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