Ocular albinism 26399002
SNOMED CT code
SNOMED code | 26399002 |
---|---|
name | Ocular albinism |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Ocular albinism (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Eye structure 81745001 |
Associated morphology | Decreased melanin pigmentation 37257004 |
parents | |
children | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Albinism 15890002 Ocular albinism 26399002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of eye 19416009 Ocular albinism 26399002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of eye 371405004 Anomaly of eye 11131000119108 Lesion of eye 301905003 Ocular albinism 26399002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Ocular albinism 26399002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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