GNB5-related intellectual disability, cardiac arrhythmia syndrome 1186711002
SNOMED CT code
| SNOMED code | 1186711002 |
|---|---|
| name | GNB5-related intellectual disability, cardiac arrhythmia syndrome |
| status | active |
| date introduced | 2021-11-30 |
| fully specified name(s) | G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group4 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group1 | |
| Finding site | Cardiac conducting system structure 24964005 |
| 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 GNB5-related intellectual disability, cardiac arrhythmia syndrome 1186711002 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 GNB5-related intellectual disability, cardiac arrhythmia syndrome 1186711002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 GNB5-related intellectual disability, cardiac arrhythmia syndrome 1186711002 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Cardiac finding 301095005 Heart disease 56265001 Cardiac arrhythmia 698247007 Cardiac arrhythmia associated with genetic disorder 698270004 GNB5-related intellectual disability, cardiac arrhythmia syndrome 1186711002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 GNB5-related intellectual disability, cardiac arrhythmia syndrome 1186711002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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