Proteus syndrome 23150001
SNOMED CT code
| SNOMED code | 23150001 |
|---|---|
| name | Proteus syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Proteus syndrome (disorder) |
| synonyms | Proteus syndrome |
| attributes - group1 | |
| Finding site | Skeletal system structure 113192009 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Nervous system structure 25087005 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Finding site | Skin structure 39937001 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hamartoma 51398009 |
| attributes - group4 | |
| Associated morphology | Neoplasm 108369006 |
| Occurrence | Congenital 255399007 |
| Finding site | Nervous system structure 25087005 |
| attributes - group5 | |
| Associated morphology | Neoplasm 108369006 |
| Finding site | Skin structure 39937001 |
| Occurrence | Congenital 255399007 |
| parents |
|
| children | Port-wine stain in proteus syndrome 403856000 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Disorder of skeletal system 88230002 Skeletal dysplasia 105986008 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hamartoma 399960008 Congenital hamartoma of skin 400083002 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with early overgrowth 48637007 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Neurocutaneous syndrome 78572006 Proteus syndrome 23150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Congenital anomaly of nervous system 88425004 Proteus syndrome 23150001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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