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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 Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction morphologie associée (attribut) Agenesis (morphologic abnormality) false Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction localisation d'une constatation (attribut) Structure of paramesonephric duct true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction morphologie associée (attribut) Aplasia true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction est un(e) (attribut) Autosomal dominant hereditary disorder false Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction est un(e) (attribut) Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction est un(e) (attribut) Mullerian aplasia true Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction est un(e) (attribut) dysfonction ovarienne true Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction est un(e) (attribut) Reproductive system hereditary disorder true Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction survenue (attribut) congénital false Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction localisation d'une constatation (attribut) Ovarian endocrine structure false Inferred relationship Some
WNT4 Mullerian aplasia and ovarian dysfunction morphologie associée (attribut) Congenital absence false Inferred relationship Some 3
WNT4 Mullerian aplasia and ovarian dysfunction localisation d'une constatation (attribut) utérus (structure corporelle) false Inferred relationship Some 3
WNT4 Mullerian aplasia and ovarian dysfunction survenue (attribut) congénital true Inferred relationship Some 1
WNT4 Mullerian aplasia and ovarian dysfunction localisation d'une constatation (attribut) utérus (structure corporelle) false Inferred relationship Some 1
WNT4 Mullerian aplasia and ovarian dysfunction morphologie associée (attribut) Congenital absence false Inferred relationship Some 1
WNT4 Mullerian aplasia and ovarian dysfunction survenue (attribut) congénital true Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction morphologie associée (attribut) Congenital absence false Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction localisation d'une constatation (attribut) Entire uterus false Inferred relationship Some 2
WNT4 Mullerian aplasia and ovarian dysfunction localisation d'une constatation (attribut) Ovarian endocrine structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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