Manitoba oculotrichoanal syndrome 703539006
SNOMED CT code
SNOMED code | 703539006 |
---|---|
name | Manitoba oculotrichoanal syndrome |
status | active |
date introduced | 2014-07-31 |
fully specified name(s) | Manitoba oculotrichoanal syndrome (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Manitoba oculotrichoanal syndrome 703539006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Manitoba oculotrichoanal syndrome 703539006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Manitoba oculotrichoanal syndrome 703539006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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