11q22.2q22.3 microdeletion syndrome 1229882003
SNOMED CT code
SNOMED code | 1229882003 |
---|---|
name | 11q22.2q22.3 microdeletion syndrome |
status | active |
date introduced | 2022-05-31 |
fully specified name(s) | 11q22.2q22.3 microdeletion syndrome (disorder) |
synonyms |
|
attributes - group4 | |
Interprets | Body height measure 50373000 |
Has interpretation | Below reference range 281300000 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Chromosome pair 11 16312006 |
Associated morphology | Partial monosomy 371169004 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Finding site | Face structure 89545001 |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Finding site | Chromosome pair 11 16312006 |
Associated morphology | Deletion of long arm 64329008 |
attributes - group5 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
attributes - group6 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 11q22.2q22.3 microdeletion syndrome 1229882003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 11q22.2q22.3 microdeletion syndrome 1229882003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental delay 248290002 11q22.2q22.3 microdeletion syndrome 1229882003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 11 60891003 Deletion of part of chromosome 11 726381002 11q partial monosomy syndrome 4325000 11q22.2q22.3 microdeletion syndrome 1229882003 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 11q22.2q22.3 microdeletion syndrome 1229882003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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