Male infertility of chromosomal origin 236791009
SNOMED CT code
SNOMED code | 236791009 |
---|---|
name | Male infertility of chromosomal origin |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Male infertility of chromosomal origin (disorder) |
synonyms | Male infertility of chromosomal origin |
attributes - group3 | |
Interprets | Fertility, function 397594008 |
attributes - group2 | |
Due to | Chromosomal disorder 409709004 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Male genital structure 90264002 |
parents | Congenital male infertility 236790005 |
children | Sensorineural deafness and male infertility 700489002 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital male infertility 236790005 Male infertility of chromosomal origin 236791009 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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