Wellesley Carman French syndrome 715988005
SNOMED CT code
| SNOMED code | 715988005 |
|---|---|
| name | Wellesley Carman French syndrome |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Cataract with aberrant oral frenula and growth delay syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Lens clear 78076003 |
| Associated morphology | Opacity 128305008 |
| attributes - group2 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Face structure 89545001 |
| attributes - group3 | |
| Interprets | Height / growth measure 271603002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Wellesley Carman French syndrome 715988005 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Wellesley Carman French syndrome 715988005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Wellesley Carman French syndrome 715988005 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Wellesley Carman French syndrome 715988005 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 Wellesley Carman French syndrome 715988005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disorder of eye 62585004 Cataract 193570009 Congenital cataract 79410001 Wellesley Carman French syndrome 715988005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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