Primary CD59 deficiency 778027003
SNOMED CT code
| SNOMED code | 778027003 | ||
|---|---|---|---|
| name | Primary CD59 deficiency | ||
| status | active | ||
| date introduced | 2019-01-31 | ||
| fully specified name(s) | Primary CD59 deficiency (disorder) | ||
| synonyms | Primary CD59 deficiency | ||
| attributes - group2 | |||
| Interprets | Measurement of total hemoglobin concentration 441689006 | ||
| Has interpretation | Below reference range 281300000 | ||
| attributes - group1 | |||
| Has interpretation | Below reference range 281300000 | ||
| Interprets | Red blood cell count 14089001 | ||
| attributes - group5 | |||
| Finding site | Peripheral nerve structure 84782009 | ||
| attributes - group4 | |||
| Finding site | Erythrocyte 41898006 | ||
| attributes - group7 | |||
| Finding site | Immune system structure 116003000 | ||
| attributes - group3 | |||
| Interprets | Hemolysis 404227002 | ||
| Has interpretation | Present 52101004 | ||
| attributes - group6 | |||
| Pathological process | Abnormal immune process 769247005 | ||
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of cellular component of blood 414022008 Anemia 271737000 Hemolytic anemia 61261009 Coombs negative hemolytic anemia 12189000 Primary CD59 deficiency 778027003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of body system 362965005 Disorder of immune structure 414030009 Complement regulatory factor defect 234618008 Primary CD59 deficiency 778027003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of soft tissue 19660004 Peripheral nerve disease 302226006 Primary CD59 deficiency 778027003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 Primary CD59 deficiency 778027003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Primary CD59 deficiency 778027003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of cellular component of blood 414022008 Red blood cell disorder 38292009 Hereditary red blood cell disorder 414394009 Primary CD59 deficiency 778027003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Primary CD59 deficiency 778027003 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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