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1332509007: fragiele-X-geassocieerde primaire ovariuminsufficiëntie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5354686016 Fragile X associated primary ovarian insufficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5354687013 Fragile X associated primary ovarian insufficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
15103681000146116 fragiele-X-geassocieerde primaire ovariuminsufficiëntie (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15103691000146119 fragiele-X-gerelateerde primaire ovariële insufficiëntie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15103701000146119 fragiele-X-geassocieerde primaire ovariuminsufficiëntie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15103711000146117 FXPOI nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5354688015 A rare, genetic premature ovarian failure characterised by decreased, abnormal or loss of ovarian function prior to age 40 in women bearing a premutation in FMR1 gene. This is defined as an expansion of 55-200 CGG repeats in the 5' untranslated region of the FMR1 gene. Clinical features include irregular or absent menstrual cycles (amenorrhoea), irregular ovulation and altered hormone profile (hypooestrogenism, and elevated serum gonadotropin levels) associated to fragile X premutation. Most of the patients have fertility problems (subfertility or infertility) and undergo early menopause. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5354689011 A rare, genetic premature ovarian failure characterized by decreased, abnormal or loss of ovarian function prior to age 40 in women bearing a premutation in FMR1 gene. This is defined as an expansion of 55-200 CGG repeats in the 5' untranslated region of the FMR1 gene. Clinical features include irregular or absent menstrual cycles (amenorrhea), irregular ovulation and altered hormone profile (hypoestrogenism, and elevated serum gonadotropin levels) associated to fragile X premutation. Most of the patients have fertility problems (subfertility or infertility) and undergo early menopause. en Definition 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
Fragile X associated primary ovarian insufficiency Is a Premature ovarian failure true Inferred relationship Some
Fragile X associated primary ovarian insufficiency Is a Genetic disease true Inferred relationship Some
Fragile X associated primary ovarian insufficiency Finding site Ovarian endocrine structure true Inferred relationship Some 2
Fragile X associated primary ovarian insufficiency Interprets Hormone secretion true Inferred relationship Some 1
Fragile X associated primary ovarian insufficiency Has interpretation Decreased true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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