Hypopigmentation-immunodeficiency disease 37548006
SNOMED CT code
SNOMED code | 37548006 |
---|---|
name | Hypopigmentation-immunodeficiency disease |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hypopigmentation-immunodeficiency disease (disorder) |
synonyms |
|
attributes - group3 | |
Associated morphology | Decreased melanin pigmentation 37257004 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Pathological process | Abnormal immune process 769247005 |
Occurrence | Congenital 255399007 |
Finding site | Immune system structure 116003000 |
parents | |
children |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of immune structure 414030009 Immunodeficiency with major anomalies 234631003 Immunodeficiency associated with multiple organ system abnormalities 234641000 Hypopigmentation-immunodeficiency disease 37548006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Hypopigmentation-immunodeficiency disease 37548006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 Hypopigmentation-immunodeficiency disease 37548006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of organic acid metabolism 116021002 Disorder of amino acid metabolism 44779003 Disorder of amino acid and organic acid metabolism 237911005 Disturbance of tyrosine metabolism 37200009 Hypopigmentation-immunodeficiency disease 37548006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Hypopigmentation-immunodeficiency disease 37548006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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