Minimal pigment oculocutaneous albinism 237919007
SNOMED CT code
SNOMED code | 237919007 |
---|---|
name | Minimal pigment oculocutaneous albinism |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Minimal pigment oculocutaneous albinism (disorder) |
synonyms |
|
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Decreased melanin pigmentation 37257004 |
Finding site | Skin structure 39937001 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Eye structure 81745001 |
Occurrence | Congenital 255399007 |
Associated morphology | Decreased melanin pigmentation 37257004 |
parents | Tyrosinase-negative oculocutaneous albinism 6483008 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Oculocutaneous albinism 63844009 Tyrosinase-negative oculocutaneous albinism 6483008 Minimal pigment oculocutaneous albinism 237919007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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