Shprintzen Goldberg craniosynostosis syndrome 719069008
SNOMED CT code
| SNOMED code | 719069008 |
|---|---|
| name | Shprintzen Goldberg craniosynostosis syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Shprintzen Goldberg craniosynostosis syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Face structure 89545001 |
| attributes - group1 | |
| Finding site | Joint structure of suture of skull 51863000 |
| Associated morphology | Congenital premature fusion 67798003 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Finding site | Connective tissue structure 21793004 |
| attributes - group5 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group6 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group4 | |
| Interprets | Physique type 248295007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Shprintzen Goldberg craniosynostosis syndrome 719069008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Shprintzen Goldberg craniosynostosis syndrome 719069008 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general observation of appearance 301305006 Physique finding 366209005 Marfanoid physique 248298009 Shprintzen Goldberg craniosynostosis syndrome 719069008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Musculoskeletal and connective tissue disorder 312225001 Shprintzen Goldberg craniosynostosis syndrome 719069008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Connective tissue hereditary disorder 363045008 Shprintzen Goldberg craniosynostosis syndrome 719069008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Shprintzen Goldberg craniosynostosis syndrome 719069008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Shprintzen Goldberg craniosynostosis syndrome 719069008 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 Shprintzen Goldberg craniosynostosis syndrome 719069008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Shprintzen Goldberg craniosynostosis syndrome 719069008 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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