Familial benign pemphigus 79468000
SNOMED CT code
| SNOMED code | 79468000 |
|---|---|
| name | Familial benign pemphigus |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Familial benign pemphigus (disorder) |
| synonyms |
|
| attributes - group2 | |
| Associated morphology | Acantholysis 43327007 |
| Finding site | Skin structure 39937001 |
| attributes - group1 | |
| Associated morphology | Blister 339008 |
| Finding site | Skin structure 39937001 |
| attributes - group3 | |
| Clinical course | Chronic 90734009 |
| attributes - group4 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Keratinization 44138005 |
| 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 benign pemphigus 79468000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative skin disorder 396325007 Acantholytic dermatosis 1251371002 Familial benign pemphigus 79468000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of skin 128236002 Familial benign pemphigus 79468000 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Disorder of keratinization 277905003 Inherited disorder of keratinization 254214009 Familial benign pemphigus 79468000 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Injury of integument 125592002 Blister of skin 823996003 Familial benign pemphigus 79468000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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