Rombo syndrome 721904001
SNOMED CT code
| SNOMED code | 721904001 |
|---|---|
| name | Rombo syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Rombo syndrome (disorder) |
| synonyms | Rombo syndrome |
| attributes - group1 | |
| Associated morphology | Growth alteration 57697001 |
| Finding site | Hair structure 386045008 |
| attributes - group2 | |
| Associated morphology | Atrophy 13331008 |
| Finding site | Skin structure 39937001 |
| 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 Rombo syndrome 721904001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Rombo syndrome 721904001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative skin disorder 396325007 Atrophic condition of skin 400190005 Rombo syndrome 721904001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Hair finding 247522004 Disorder of hair 279425004 Disorder of hair growth 267808001 Hypotrichosis 53602002 Rombo syndrome 721904001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Rombo syndrome 721904001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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