9q33.3q34.11 microdeletion syndrome 1228886008
SNOMED CT code
| SNOMED code | 1228886008 |
|---|---|
| name | 9q33.3q34.11 microdeletion syndrome |
| status | active |
| date introduced | 2022-05-31 |
| fully specified name(s) | 9q33.3q34.11 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 9 13526007 |
| Associated morphology | Partial monosomy 371169004 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 9 13526007 |
| 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 9q33.3q34.11 microdeletion syndrome 1228886008 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 9q33.3q34.11 microdeletion syndrome 1228886008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental delay 248290002 9q33.3q34.11 microdeletion syndrome 1228886008 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 9 5051002 Deletion of part of chromosome 9 726379004 9q partial monosomy syndrome 43420005 9q33.3q34.11 microdeletion syndrome 1228886008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 9q33.3q34.11 microdeletion syndrome 1228886008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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