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237788002: Premature ovarian failure (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356353015 Premature ovarian failure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356354014 POF - Premature ovarian failure en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
626565011 Premature ovarian failure (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1841051000195116 insufficienza ovarica precoce it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
436901000172111 insuffisance ovarienne prématurée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
886971000195110 Vorzeitige Ovarialinsuffizienz de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
886981000195112 POF - premature-ovarian-failure-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Premature ovarian failure (disorder) Is a Primary ovarian failure true Inferred relationship Some
Premature ovarian failure (disorder) Interprets Decreased hormone production false Inferred relationship Some
Premature ovarian failure (disorder) Finding site Entire endocrine ovary (body structure) false Inferred relationship Some
Premature ovarian failure (disorder) Interprets défaillance false Inferred relationship Some
Premature ovarian failure (disorder) Has definitional manifestation Decreased hormone secretion false Inferred relationship Some
Premature ovarian failure (disorder) Finding site Female genital tract false Inferred relationship Some
Premature ovarian failure (disorder) Has definitional manifestation Decreased hormone production false Inferred relationship Some
Premature ovarian failure (disorder) Finding site Ovarian endocrine structure true Inferred relationship Some 2
Premature ovarian failure (disorder) Has interpretation Decreased true Inferred relationship Some 1
Premature ovarian failure (disorder) Interprets Hormone secretion true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Family history: Early menopause (situation) Associated finding False Premature ovarian failure (disorder) Inferred relationship Some 1
Family history: Early menopause (situation) Associated finding False Premature ovarian failure (disorder) Inferred relationship Some 1
Iatrogenic premature ovarian failure (disorder) Is a True Premature ovarian failure (disorder) Inferred relationship Some
Acquired premature ovarian failure Is a False Premature ovarian failure (disorder) Inferred relationship Some
Idiopathic premature ovarian failure (disorder) Is a True Premature ovarian failure (disorder) Inferred relationship Some
A rare genetic disease characterized by sclerosing dysplasia affecting the diaphyseal and metaphyseal regions of the long bones, as well as the skull and metacarpals, in association with skin changes like those seen in ichthyosis vulgaris and premature ovarian failure with bilateral hypoplasia of the ovaries. Patients present in adulthood, primarily with swelling of the extremities and occasional mild pain in the legs. Is a True Premature ovarian failure (disorder) Inferred relationship Some
Premature ovarian failure due to autoimmune oophoritis (disorder) Is a True Premature ovarian failure (disorder) Inferred relationship Some
Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome is a rare genetic syndromic intellectual disability characterized by intellectual disability, polyneuropathy, short stature and short limbs, brachydactyly, and premature ovarian insufficiency. Only one familial case with three affected females was described and there have been no further descriptions in the literature since 1971. Is a True Premature ovarian failure (disorder) Inferred relationship Some
Ovarioleukodystrophy Is a True Premature ovarian failure (disorder) Inferred relationship Some
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. Is a True Premature ovarian failure (disorder) Inferred relationship Some

This concept is not in any reference sets

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