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699275001: WNT4 Müllerian aplasia and ovarian dysfunction (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2983507013 Biason-Lauber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2983526017 WNT4 protein deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2983527014 Mayer-Rokitansky-Küster-Hausel like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2988285017 WNT4 Müllerian aplasia and ovarian dysfunction (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3014902017 WNT4 Müllerian aplasia and ovarian dysfunction en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
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 (disorder) 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 Disorder of endocrine ovary 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 (morphologic abnormality) 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 (morphologic abnormality) 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 (morphologic abnormality) 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
WNT4 Mullerian aplasia and ovarian dysfunction Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction Associated morphology Agenesis (morphologic abnormality) 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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

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