Grant syndrome 723827003
SNOMED CT code
SNOMED code | 723827003 |
---|---|
name | Grant syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Grant syndrome (disorder) |
synonyms | Grant syndrome |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Bone structure 272673000 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dysplasia 25723000 |
attributes - group2 | |
Interprets | Bone density scan 312681000 |
Has interpretation | Above reference range 281302008 |
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 Grant syndrome 723827003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Bone finding 118953000 Disorder of bone 76069003 Dysplasia with increased bone density 254120004 Grant syndrome 723827003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Grant syndrome 723827003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Grant syndrome 723827003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Grant syndrome 723827003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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