Autosomal recessive ocular albinism 78921008
SNOMED CT code
SNOMED code | 78921008 |
---|---|
name | Autosomal recessive ocular albinism |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Autosomal recessive ocular albinism (disorder) |
synonyms |
|
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Eye structure 81745001 |
Associated morphology | Decreased melanin pigmentation 37257004 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Ocular albinism 26399002 Autosomal recessive ocular albinism 78921008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive ocular albinism 78921008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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