Familial progressive hyper and hypopigmentation 763368004
SNOMED CT code
| SNOMED code | 763368004 |
|---|---|
| name | Familial progressive hyper and hypopigmentation |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Familial progressive hyperpigmentation and hypopigmentation of skin (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skin structure 39937001 |
| Associated morphology | Pigment alteration 79644001 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Familial progressive hyper and hypopigmentation 763368004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Congenital pigmentary skin anomalies 205564003 Familial progressive hyper and hypopigmentation 763368004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Familial progressive hyper and hypopigmentation 763368004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Familial progressive hyper and hypopigmentation 763368004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Familial progressive hyper and hypopigmentation 763368004 |
| 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