STAR syndrome 723581006
SNOMED CT code
| SNOMED code | 723581006 |
|---|---|
| name | STAR syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Syndactyly, telecanthus, anogenital and renal malformation syndrome (disorder) |
| synonyms |
|
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Urogenital structure 21514008 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of palpebral fissure 595000 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Anal structure 53505006 |
| Associated morphology | Congenital atresia 56457002 |
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Congenital abnormal fusion 37764001 |
| Finding site | Toe structure 29707007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked dominant hereditary disease 1162984000 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Anal finding 249628000 Disorder of anus 32110003 Congenital anomaly of anus 11194003 Anal atresia 204712000 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Multiple malformation syndrome with facial-limb defects as major feature 23359005 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Palpebral fissure finding 386656009 Telecanthus 246803005 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of the genitourinary system 42030000 Genitourinary congenital anomalies 287085006 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Disorder of digit 128597007 Congenital anomaly of digit 403855001 Syndactyly 373413006 Syndactyly of toes 32113001 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 STAR syndrome 723581006 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Disorder of eyelid 60113004 Congenital anomaly of eyelid 91158006 STAR syndrome 723581006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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