Stickler syndrome type 1 1010668008
SNOMED CT code
SNOMED code | 1010668008 |
---|---|
name | Stickler syndrome type 1 |
status | active |
date introduced | 2021-01-31 |
fully specified name(s) | Stickler syndrome type 1 (disorder) |
synonyms | Stickler syndrome type 1 |
attributes - group1 | |
Finding site | Joint structure 39352004 |
Occurrence | Congenital 255399007 |
Associated morphology | Degenerative abnormality 107669003 |
Pathological process | Pathological developmental process 308490002 |
attributes - group2 | |
Associated morphology | Dysplasia 25723000 |
Finding site | Bone structure 272673000 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Vitreous body structure 47538007 |
Pathological process | Pathological developmental process 308490002 |
attributes - group4 | |
Finding site | Retinal structure 5665001 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
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 Stickler syndrome type 1 1010668008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Musculoskeletal and connective tissue disorder 312225001 Stickler syndrome 78675000 Stickler syndrome type 1 1010668008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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