Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006
SNOMED CT code
SNOMED code | 733457006 |
---|---|
name | Ehlers-Danlos and osteogenesis imperfecta syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Ehlers-Danlos and osteogenesis imperfecta syndrome (disorder) |
synonyms | Ehlers-Danlos and osteogenesis imperfecta syndrome |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Bone structure 272673000 |
Associated morphology | Dysplasia 25723000 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Skin structure 39937001 |
Associated morphology | Dysplasia 25723000 |
attributes - group4 | |
Finding site | Connective tissue structure 21793004 |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
attributes - group3 | |
Interprets | Bone formation 83323007 |
Has interpretation | Abnormal 263654008 |
attributes - group6 | |
Interprets | Bone density scan 312681000 |
Has interpretation | Below reference range 281300000 |
attributes - group7 | |
Interprets | Range of joint movement 364564000 |
Has interpretation | Above reference range 281302008 |
attributes - group5 | |
Finding site | Joint structure 39352004 |
parents |
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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 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Procedure related finding 127325009 Bone density finding 385342005 Bone density below reference range 449781000 Dysplasia with decreased bone density 254104009 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Musculoskeletal and connective tissue disorder 312225001 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Congenital connective tissue disorder 363039000 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Connective tissue hereditary disorder 363045008 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Joint finding 118952005 Arthropathy 399269003 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Abnormal bone formation 36123008 Osteogenesis imperfecta 78314001 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Joint finding 118952005 Hypermobility of joint 788453008 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 SNOMED CT Concept 138875005 Clinical finding 404684003 General finding of soft tissue 248402002 Disorder of soft tissue 19660004 Soft tissue lesion 239953001 Skin lesion 95324001 Ehlers-Danlos and osteogenesis imperfecta syndrome 733457006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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