Familial isolated congenital asplenia 726708009
SNOMED CT code
| SNOMED code | 726708009 |
|---|---|
| name | Familial isolated congenital asplenia |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Familial isolated congenital asplenia (disorder) |
| synonyms | Familial isolated congenital asplenia |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Absence 418560003 |
| Occurrence | Congenital 255399007 |
| Finding site | Splenic structure 78961009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Familial isolated congenital asplenia 726708009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial isolated congenital asplenia 726708009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Familial isolated congenital asplenia 726708009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Familial isolated congenital asplenia 726708009 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of spleen 51244008 Asplenia 707147002 Congenital absence of spleen 93030006 Familial isolated congenital asplenia 726708009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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