Grubben, De Cock, Borghgraef syndrome 763186006
SNOMED CT code
| SNOMED code | 763186006 |
|---|---|
| name | Grubben, De Cock, Borghgraef syndrome |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Grubben, De Cock, Borghgraef syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group3 | |
| Interprets | Adaptation behavior 406208005 |
| 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 Grubben, De Cock, Borghgraef syndrome 763186006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Grubben, De Cock, Borghgraef syndrome 763186006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Grubben, De Cock, Borghgraef syndrome 763186006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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