Muenke syndrome 787407003
SNOMED CT code
| SNOMED code | 787407003 |
|---|---|
| name | Muenke syndrome |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Muenke syndrome (disorder) |
| synonyms | Muenke syndrome |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of coronal suture of skull 29012004 |
| Associated morphology | Congenital premature fusion 67798003 |
| 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 Muenke syndrome 787407003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Muenke syndrome 787407003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Muenke syndrome 787407003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Muenke syndrome 787407003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Joint finding 118952005 Cranial suture finding 248387005 Imperfect fusion of skull 23939000 Craniosynostosis syndrome 57219006 Fibroblast growth factor receptor 3-related craniosynostosis 440350001 Muenke syndrome 787407003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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