Wiedemann Steiner syndrome 763618001
SNOMED CT code
| SNOMED code | 763618001 |
|---|---|
| name | Wiedemann Steiner syndrome |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Wiedemann Steiner syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Face structure 89545001 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Growth alteration 57697001 |
| Finding site | Hair structure 386045008 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Interprets | Height / growth measure 271603002 |
| 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 Wiedemann Steiner syndrome 763618001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Wiedemann Steiner syndrome 763618001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Wiedemann Steiner syndrome 763618001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Wiedemann Steiner syndrome 763618001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Congenital anomaly of hair 65033000 Congenital hypertrichosis 56797000 Wiedemann Steiner syndrome 763618001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Wiedemann Steiner syndrome 763618001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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