FRAXE intellectual disability syndrome 716709002
SNOMED CT code
| SNOMED code | 716709002 |
|---|---|
| name | FRAXE intellectual disability syndrome |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | FRAXE intellectual disability syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Chromosomal morphology 107675007 |
| Occurrence | Congenital 255399007 |
| Finding site | Sex chromosome X 72837006 |
| 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 FRAXE intellectual disability syndrome 716709002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 FRAXE intellectual disability syndrome 716709002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of sex chromosome 95462004 Anomaly of chromosome X 111312006 Fragile X chromosome 205720009 FRAXE intellectual disability syndrome 716709002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 FRAXE intellectual disability syndrome 716709002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 FRAXE intellectual disability syndrome 716709002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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