HNSHA due to triosephosphate isomerase deficiency 44641000
SNOMED CT code
SNOMED code | 44641000 |
---|---|
name | HNSHA due to triosephosphate isomerase deficiency |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) |
synonyms |
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attributes - group3 | |
Has interpretation | Present 52101004 |
Interprets | Hemolysis 404227002 |
attributes - group5 | |
Due to | Triose phosphate isomerase deficiency 234405009 |
attributes - group1 | |
Has interpretation | Below reference range 281300000 |
Interprets | Red blood cell count 14089001 |
attributes - group2 | |
Has interpretation | Below reference range 281300000 |
Interprets | Measurement of total hemoglobin concentration 441689006 |
attributes - group4 | |
Finding site | Erythrocyte 41898006 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 Hemolytic disorder 128086004 Hemolytic anemia 61261009 Anemia due to enzyme deficiency 111577008 HNSHA due to triosephosphate isomerase deficiency 44641000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 HNSHA due to triosephosphate isomerase deficiency 44641000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Red blood cell disorder 38292009 Erythrocyte enzyme deficiency 234401000 HNSHA due to triosephosphate isomerase deficiency 44641000 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 Hereditary hemolytic anemia 38911009 Hereditary nonspherocytic hemolytic anemia 301317008 HNSHA due to triosephosphate isomerase deficiency 44641000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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