X-linked reticulate pigmentary disorder with systemic manifestation syndrome 717224002
SNOMED CT code
| SNOMED code | 717224002 |
|---|---|
| name | X-linked reticulate pigmentary disorder with systemic manifestation syndrome |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) |
| synonyms |
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| attributes - group1 | |
| Associated morphology | Hyperpigmentation 4830009 |
| Finding site | Skin structure 39937001 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked dominant hereditary disease 1162984000 X-linked reticulate pigmentary disorder with systemic manifestation syndrome 717224002 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 X-linked reticulate pigmentary disorder with systemic manifestation syndrome 717224002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Hyperpigmentation of skin 49765009 X-linked reticulate pigmentary disorder with systemic manifestation syndrome 717224002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 X-linked reticulate pigmentary disorder with systemic manifestation syndrome 717224002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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