Phylloid hypomelanosis 403807001
SNOMED CT code
| SNOMED code | 403807001 |
|---|---|
| name | Phylloid hypomelanosis |
| status | active |
| date introduced | 2003-07-31 |
| fully specified name(s) | Phylloid hypomelanosis (disorder) |
| synonyms | Phylloid hypomelanosis |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skin structure 39937001 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Decreased melanin pigmentation 37257004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Albinism 15890002 Phylloid hypomelanosis 403807001 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 Phylloid hypomelanosis 403807001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Phylloid hypomelanosis 403807001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Phylloid hypomelanosis 403807001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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