Congenital anomaly of cartilage 67988000 SNOMED CT code SNOMED code 67988000 name Congenital anomaly of cartilage status active date introduced 2002-01-31 fully specified name(s) Congenital anomaly of cartilage (disorder) synonyms Congenital anomaly of cartilage Chondrodystrophy Abnormal development of cartilage attributes - group1 Finding site Cartilage structure 771314001 Pathological process Pathological developmental process 308490002 Associated morphology Morphologically abnormal structure 49755003 Occurrence Congenital 255399007 parents Congenital connective tissue disorder 363039000 Cartilage disorder 50927007 Congenital anomaly of musculoskeletal system 73573004 children Agenesis of nasal cartilages 232381002 Cleft cartilaginous centrum of lumbar vertebra 92490007 Cleft cartilaginous centrum of sacral vertebra 92491006 Cleft cartilaginous centrum of thoracic vertebra 92492004 Congenital abnormal fusion of centrum cartilage of lumbar vertebra 92845005 Congenital abnormal fusion of centrum cartilage of sacral vertebra 92846006 Congenital abnormal fusion of centrum cartilage of thoracic vertebra 92847002 Congenital anomaly of cricoid cartilage 23061007 Congenital anomaly of rib cartilage 93022005 Congenital anomaly of thyroid cartilage 8032007 Congenital anomaly of tracheal cartilage 42666000 Congenital bronchomalacia 95468000 Congenital cartilage anomaly of third eyelid 95511000 removed: 2014-01-31 Congenital discoid meniscus 70690000 Congenital laryngomalacia 253737007 Disorganized development of cartilaginous and fibrous components of the skeleton 254140006 Dumbbell-shaped cartilaginous centrum of cervical vertebra 93441003 Dumbbell-shaped cartilaginous centrum of lumbar vertebra 93442005 Dumbbell-shaped cartilaginous centrum of sacral vertebra 93443000 Dumbbell-shaped cartilaginous centrum of thoracic vertebra 93444006 Hypoplasia and coloboma of alar cartilage with telecanthus syndrome 722284009 Keutel syndrome 724208006 Metaphyseal chondrodysplasia, McKusick type 7720002 Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome 766821006 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Congenital connective tissue disorder 363039000 Congenital anomaly of cartilage 67988000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Cartilage finding 118954006 Cartilage disorder 50927007 Congenital anomaly of cartilage 67988000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Congenital anomaly of musculoskeletal system 73573004 Congenital anomaly of cartilage 67988000 ancestors sorted most to least specific
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