WNT4 Mullerian aplasia and ovarian dysfunction 699275001
SNOMED CT code
| SNOMED code | 699275001 |
|---|---|
| name | WNT4 Mullerian aplasia and ovarian dysfunction |
| status | active |
| date introduced | 2014-01-31 |
| fully specified name(s) | WNT4 Müllerian aplasia and ovarian dysfunction (disorder) |
| synonyms |
|
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Structure of paramesonephric duct 26896004 |
| Associated morphology | Aplasia 45486003 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Ovarian endocrine structure 304043001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Mullerian aplasia 253828000 WNT4 Mullerian aplasia and ovarian dysfunction 699275001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 WNT4 Mullerian aplasia and ovarian dysfunction 699275001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 WNT4 Mullerian aplasia and ovarian dysfunction 699275001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Disorder of endocrine gonad 127345001 Disorder of endocrine ovary 37102008 WNT4 Mullerian aplasia and ovarian dysfunction 699275001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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