Intellectual disability, developmental delay, contracture syndrome 722456001
SNOMED CT code
| SNOMED code | 722456001 |
|---|---|
| name | Intellectual disability, developmental delay, contracture syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Intellectual disability, developmental delay, contracture syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Contracture 57048009 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Structure of joint region 785818007 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skeletal muscle structure 127954009 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Atrophy 13331008 |
| attributes - group3 | |
| Interprets | Range of joint movement 364564000 |
| Has interpretation | Decreased 1250004 |
| attributes - group4 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group5 | |
| 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 Intellectual disability, developmental delay, contracture syndrome 722456001 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 Intellectual disability, developmental delay, contracture syndrome 722456001 SNOMED CT Concept 138875005 Clinical finding 404684003 Deformity 417893002 Congenital deformity 276655000 Arthrogryposis 111246005 Arthrogryposis multiplex congenita 205402004 Intellectual disability, developmental delay, contracture syndrome 722456001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Inherited arthrogryposis 28204005 Intellectual disability, developmental delay, contracture syndrome 722456001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Intellectual disability, developmental delay, contracture syndrome 722456001 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Degenerative disorder of muscle 363058009 Muscle atrophy 88092000 Intellectual disability, developmental delay, contracture syndrome 722456001 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Congenital anomaly of skeletal muscle 89886004 Intellectual disability, developmental delay, contracture syndrome 722456001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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