Albinism 15890002
SNOMED CT code
| SNOMED code | 15890002 |
|---|---|
| name | Albinism |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Albinism (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Decreased melanin pigmentation 37257004 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Albinism 15890002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Albinism 15890002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Albinism 15890002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Albinism 15890002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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