Griscelli syndrome type 1 1254946006
SNOMED CT code
SNOMED code | 1254946006 |
---|---|
name | Griscelli syndrome type 1 |
status | active |
date introduced | 2022-10-31 |
fully specified name(s) | Hypopigmentation-immunodeficiency disease type 1 (disorder) |
synonyms |
|
attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Decreased melanin pigmentation 37257004 |
Pathological process | Pathological developmental process 308490002 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Finding site | Immune system structure 116003000 |
Pathological process | Pathological developmental process 308490002 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Finding site | Immune system structure 116003000 |
Pathological process | Abnormal immune process 769247005 |
parents | Hypopigmentation-immunodeficiency disease 37548006 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Hypopigmentation-immunodeficiency disease 37548006 Griscelli syndrome type 1 1254946006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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