X-linked dominant chondrodysplasia Chassaing Lacombe type 719837003
SNOMED CT code
SNOMED code | 719837003 |
---|---|
name | X-linked dominant chondrodysplasia Chassaing Lacombe type |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) |
synonyms | X-linked dominant chondrodysplasia Chassaing Lacombe type |
attributes - group1 | |
Finding site | Bone structure 272673000 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Dysplasia 25723000 |
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 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked dominant hereditary disease 1162984000 X-linked dominant chondrodysplasia Chassaing Lacombe type 719837003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Chondrodysplasia 205465004 X-linked dominant chondrodysplasia Chassaing Lacombe type 719837003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 X-linked dominant chondrodysplasia Chassaing Lacombe type 719837003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 X-linked dominant chondrodysplasia Chassaing Lacombe type 719837003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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