Pfeiffer syndrome type 1 1003877009
SNOMED CT code
SNOMED code | 1003877009 |
---|---|
name | Pfeiffer syndrome type 1 |
status | active |
date introduced | 2021-01-31 |
fully specified name(s) | Pfeiffer syndrome type 1 (disorder) |
synonyms | Pfeiffer syndrome type 1 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Congenital abnormal fusion 37764001 |
Finding site | Digit structure 82680008 |
attributes - group2 | |
Associated morphology | Congenital premature fusion 67798003 |
Occurrence | Congenital 255399007 |
Finding site | Joint structure of suture of skull 51863000 |
Pathological process | Pathological developmental process 308490002 |
parents | Acrocephalosyndactyly type V 70410008 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Acrocephalosyndactyly 268262006 Acrocephalosyndactyly type V 70410008 Pfeiffer syndrome type 1 1003877009 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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