Hereditary anetoderma 733467001
SNOMED CT code
| SNOMED code | 733467001 |
|---|---|
| name | Hereditary anetoderma |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Hereditary anetoderma (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Focal atrophy with macular pattern 1296525001 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| 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 Hereditary anetoderma 733467001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Hereditary anetoderma 733467001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative skin disorder 396325007 Atrophic condition of skin 400190005 Anetoderma 238828009 Hereditary anetoderma 733467001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Hereditary anetoderma 733467001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Hereditary anetoderma 733467001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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