SCALP syndrome 774208009
SNOMED CT code
| SNOMED code | 774208009 |
|---|---|
| name | SCALP syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome (disorder) |
| synonyms |
|
| attributes - group3 | |
| Associated morphology | Epidermal nevus 25201003 |
| Finding site | Skin structure 39937001 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skin part 119181002 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Aplasia 45486003 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Central nervous system structure 21483005 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 SCALP syndrome 774208009 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 Aplasia cutis congenita 35484002 SCALP syndrome 774208009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hamartoma 399960008 Congenital hamartoma of skin 400083002 SCALP syndrome 774208009 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Hamartoma of integument 400206003 Hamartoma of skin 399921006 Epidermal nevus 239107007 Sebaceous nevus 707136009 SCALP syndrome 774208009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 SCALP syndrome 774208009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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