Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008
SNOMED CT code
| SNOMED code | 724016008 |
|---|---|
| name | Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome (disorder) |
| synonyms | Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome |
| attributes - group1 | |
| Finding site | Lower lacrimal punctum 263346001 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Absence 418560003 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Prolapse 29696001 |
| Finding site | Upper eyelid structure 38934000 |
| Occurrence | Congenital 255399007 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Lid margin finding 246845007 Lacrimal punctum finding 246855006 Lower lacrimal punctum finding 246857003 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Disorder of eyelid 60113004 Ptosis of eyelid 11934000 Congenital ptosis 268163008 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Lacrimal system finding 416270005 Lacrimal drainage pathway finding 246854005 Disorder of lacrimal passage 27091000119107 Congenital abnormality of lacrimal drainage system 420049001 Congenital absence of lacrimal drainage structure 418087009 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Lid margin finding 246845007 Lacrimal punctum finding 246855006 Dysgenesis of lacrimal punctum 422731002 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Disorder of eyelid 60113004 Congenital anomaly of eyelid 91158006 Ablepharon 13401001 Partial ablepharon 45484000 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 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 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome 724016008 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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