Infantile systemic hyalinosis 238867003
SNOMED CT code
| SNOMED code | 238867003 |
|---|---|
| name | Infantile systemic hyalinosis |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Infantile systemic hyalinosis (disorder) |
| synonyms | Infantile systemic hyalinosis |
| attributes - group1 | |
| Associated morphology | Fibromatosis 19928005 |
| Finding site | Skin structure 39937001 |
| attributes - group3 | |
| Finding site | Joint structure 39352004 |
| Associated morphology | Contracture 57048009 |
| attributes - group5 | |
| Associated morphology | Hyaline degeneration 19010006 |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure 272673000 |
| Associated morphology | Fibrous dysplasia 789439000 |
| attributes - group2 | |
| Finding site | Bone structure 272673000 |
| Associated morphology | Osteolysis 30425001 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Fibromatosis 723976005 Hyaline fibromatosis syndrome 1197494003 Infantile systemic hyalinosis 238867003 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Infantile systemic hyalinosis 238867003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Infantile systemic hyalinosis 238867003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Infantile systemic hyalinosis 238867003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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