Amelo-onycho-hypohidrotic syndrome 715404000
SNOMED CT code
| SNOMED code | 715404000 |
|---|---|
| name | Amelo-onycho-hypohidrotic syndrome |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Ameloonychohypohidrotic syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| Occurrence | Congenital 255399007 |
| Finding site | Ectoderm structure 63206006 |
| 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 Amelo-onycho-hypohidrotic syndrome 715404000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Amelo-onycho-hypohidrotic syndrome 715404000 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Amelo-onycho-hypohidrotic syndrome 715404000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Amelo-onycho-hypohidrotic syndrome 715404000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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