Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006
SNOMED CT code
SNOMED code | 766821006 |
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name | Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome (disorder) |
synonyms | Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome |
attributes - group4 | |
Finding site | Cartilage structure 771314001 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Pathologic calcification 18115005 |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Finding site | Face structure 89545001 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dysplasia 25723000 |
Occurrence | Congenital 255399007 |
Finding site | Bone structure 272673000 |
attributes - group3 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Abnormally short growth 11182007 |
Finding site | Entire limb 243996003 |
attributes - group5 | |
Interprets | Height / growth measure 271603002 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Multiple malformation syndrome with facial-limb defects as major feature 23359005 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Calcinosis 6595006 Chondrocalcinosis 239838005 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Metaphyseal chondrodysplasia 28681006 Spondyloepimetaphyseal disorder 254062008 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Connective tissue hereditary disorder 363045008 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Deformity of limb 445144002 Longitudinal deficiency of limb 67341007 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Congenital connective tissue disorder 363039000 Congenital anomaly of cartilage 67988000 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Cartilage finding 118954006 Cartilage disorder 50927007 Osteochondropathy 77881008 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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