Piebaldism 718122005
SNOMED CT code
| SNOMED code | 718122005 |
|---|---|
| name | Piebaldism |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Piebaldism (disorder) |
| synonyms | Piebaldism |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Hypopigmentation 89031001 |
| 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 Autosomal dominant hereditary disorder 11164009 Piebaldism 718122005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Skin hypopigmented 23006000 Congenital deficiency of pigment of skin 1953005 Piebaldism 718122005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Piebaldism 718122005 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Piebaldism 718122005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Piebaldism 718122005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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