Mayer-Rokitansky-Küster-Hauser syndrome type 2 717705004
SNOMED CT code
SNOMED code | 717705004 |
---|---|
name | Mayer-Rokitansky-Küster-Hauser syndrome type 2 |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) |
synonyms |
|
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Structure of upper third of vagina 29038004 |
Associated morphology | Absence 418560003 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Uterine structure 35039007 |
Occurrence | Congenital 255399007 |
Associated morphology | Absence 418560003 |
attributes - group3 | |
Finding site | Structure of middle third of vagina 38121002 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Absence 418560003 |
parents | Rokitansky sequence 8793008 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Malformation sequence 105989001 Rokitansky sequence 8793008 Mayer-Rokitansky-Küster-Hauser syndrome type 2 717705004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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