Acrocephalosyndactyly type V 70410008
SNOMED CT code
SNOMED code | 70410008 |
---|---|
name | Acrocephalosyndactyly type V |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Acrocephalosyndactyly type V (disorder) |
synonyms |
|
attributes - group2 | |
Associated morphology | Congenital abnormal fusion 37764001 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Digit structure 82680008 |
Occurrence | Congenital 255399007 |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Congenital premature fusion 67798003 |
Occurrence | Congenital 255399007 |
Finding site | Joint structure of suture of skull 51863000 |
parents | |
children |
|
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 Acrocephalosyndactyly type V 70410008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Acrocephalosyndactyly 268262006 Acrocephalosyndactyly type V 70410008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Acrocephalosyndactyly type V 70410008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Acrocephalosyndactyly type V 70410008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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