Parietal foramina with clavicular hypoplasia 771338002
SNOMED CT code
SNOMED code | 771338002 |
---|---|
name | Parietal foramina with clavicular hypoplasia |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Parietal foramina with clavicular hypoplasia (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Bone structure of cranium 89546000 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
attributes - group3 | |
Finding site | Bone structure 272673000 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dysplasia 25723000 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Finding site | Bone structure of clavicle 51299004 |
Associated morphology | Hypoplasia 55199003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Disorder of skeletal system 88230002 Skeletal dysplasia 105986008 Parietal foramina with clavicular hypoplasia 771338002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Parietal foramina with clavicular hypoplasia 771338002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of skull 118945008 Congenital anomaly of skull 51655004 Localized congenital skull defect 270519009 Craniolacunia 29307005 Parietal foramina with clavicular hypoplasia 771338002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Parietal foramina with clavicular hypoplasia 771338002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Parietal foramina with clavicular hypoplasia 771338002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body wall 399986003 Congenital anomaly of body wall 363027008 Congenital hypoplasia of clavicle 93250003 Parietal foramina with clavicular hypoplasia 771338002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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