Incontinentia pigmenti syndrome 367520004
SNOMED CT code
| SNOMED code | 367520004 |
|---|---|
| name | Incontinentia pigmenti syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Incontinentia pigmenti syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Finding site | Tooth structure 38199008 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Finding site | Ectoderm structure 63206006 |
| Associated morphology | Dysplasia 25723000 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Hair structure 386045008 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Finding site | Nail unit structure 770802007 |
| 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 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hereditary disorder of tooth 1148766007 Incontinentia pigmenti syndrome 367520004 SNOMED CT Concept 138875005 Clinical 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 Incontinentia pigmenti syndrome 367520004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Ectodermal dysplasia with hair-tooth defects 239027006 Ectodermal dysplasia with hair-tooth-nail defects 239015008 Incontinentia pigmenti syndrome 367520004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Incontinentia pigmenti syndrome 367520004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Incontinentia pigmenti syndrome 367520004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of nail 402775007 Incontinentia pigmenti syndrome 367520004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com