Agnathia, holoprosencephaly, situs inversus syndrome 722283003
SNOMED CT code
SNOMED code | 722283003 |
---|---|
name | Agnathia, holoprosencephaly, situs inversus syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Agnathia, holoprosencephaly, situs inversus syndrome (disorder) |
synonyms | Agnathia, holoprosencephaly, situs inversus syndrome |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Bone structure of mandible 91609006 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Hypoplasia 55199003 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Congenital anomaly of head 87290003 Holoprosencephaly sequence 30915001 Agnathia, holoprosencephaly, situs inversus syndrome 722283003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of jaw 37156001 Congenital anomaly of jaw 95473006 Congenital anomaly of mandible 128224008 Congenital micrognathism 32958008 Agnathia, holoprosencephaly, situs inversus syndrome 722283003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Agnathia, holoprosencephaly, situs inversus syndrome 722283003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Agnathia, holoprosencephaly, situs inversus syndrome 722283003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Agnathia, holoprosencephaly, situs inversus syndrome 722283003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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