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699275001: WNT4 Müllerian aplasia and ovarian dysfunction (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2983485017 WNT4 Mullerian aplasia and ovarian dysfunction en Synonym Active Case sensitive SNOMED CT core
2983507013 Biason-Lauber syndrome en Synonym Active Case sensitive SNOMED CT core
2983526017 WNT4 protein deficiency en Synonym Active Case sensitive SNOMED CT core
2983527014 Mayer-Rokitansky-Küster-Hausel like syndrome en Synonym Active Case sensitive SNOMED CT core
2988285017 WNT4 Müllerian aplasia and ovarian dysfunction (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3014902017 WNT4 Müllerian aplasia and ovarian dysfunction en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
WNT4 Mullerian aplasia and ovarian dysfunction Pathological process Pathological developmental process true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction Associated morphology Agenesis false Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction Finding site Structure of paramesonephric duct true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction Associated morphology Aplasia true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction Is a Autosomal dominant hereditary disorder false Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction Is a Hereditary disorder of endocrine system true Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction Is a Mullerian aplasia true Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction Is a Ovarian dysfunction true Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction Is a Reproductive system hereditary disorder true Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction Occurrence Congenital false Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction Finding site Ovarian endocrine structure false Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction Associated morphology Congenital absence false Inferred relationship Some 3
WNT4 Mullerian aplasia and ovarian dysfunction Finding site Uterine structure false Inferred relationship Some 3
WNT4 Mullerian aplasia and ovarian dysfunction Occurrence Congenital true Inferred relationship Some 1
WNT4 Mullerian aplasia and ovarian dysfunction Finding site Uterine structure false Inferred relationship Some 1
WNT4 Mullerian aplasia and ovarian dysfunction Associated morphology Congenital absence false Inferred relationship Some 1
WNT4 Mullerian aplasia and ovarian dysfunction Occurrence Congenital true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction Associated morphology Congenital absence false Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction Finding site Entire uterus false Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction Finding site Ovarian endocrine structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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