Congenital lethal erythroderma 722391005
SNOMED CT code
| SNOMED code | 722391005 |
|---|---|
| name | Congenital lethal erythroderma |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Congenital lethal erythroderma (disorder) |
| synonyms | Congenital lethal erythroderma |
| attributes - group1 | |
| Associated morphology | Inflammatory morphology 409774005 |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Exfoliative erythema 125118008 |
| Finding site | Skin structure 39937001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Congenital lethal erythroderma 722391005 SNOMED CT Concept 138875005 Clinical finding 404684003 Erythema 247441003 Erythema of skin 444827008 Erythroderma 399992009 Congenital lethal erythroderma 722391005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital lethal erythroderma 722391005 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Disorder of skin 95320005 Inflammatory dermatosis 703938007 Congenital lethal erythroderma 722391005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital lethal erythroderma 722391005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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