raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98310

OBSOLETE: Male infertility with impaired virilization due to an hypothalamic or pituitary disorder

inactive · referred to ORPHA:399572Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder

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Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Male infertility with impaired virilization due to an hypothalamic or pituitary disorder
frOBSOLETE : Infertilité masculine avec défaut de virilisation due à une anomalie pituitaire ou hypothalamique
deOBSOLET: Männliche Infertilität mit gestörter Virilisierung bei Hypothalamus- oder Hypophysendefekt
esOBSOLETO: Infertilidad masculina con deficiencia de virilización por defecto hipotalámico o de la hipófisis
itOBSOLETO: Sterilità maschile con virilizzazione anomala da difetti ipofisari o ipotalamici
nlOBSOLEET: Mannelijke onvruchtbaarheid met verminderde virilisatie als gevolg van een hypothalamische of hypofysaire stoornis
ptOBSOLETO: Infertilidade masculina com compromisso da virilização por doença hipotalâmica ou da pituitária
plNIEAKTUALNE: Nieplodnosc meska z uposledzona wirylizacja z powodu zaburzen podwzgórza lub przysadki
csNEAKTUÁLNÍ: Mužská neplodnost s poruchou virilizace způsobená poruchou hypotalamu nebo hypofýzy
ukЗАСТАРІЛО: Чоловіче безпліддя з порушенням вірилізації через розлади гіпоталамуса або гіпофіза.
zh弃用:下丘脑或垂体障碍所致男性不育症伴男性第二性征缺陷
trEski adı: Hipotalamik veya hipofiz hastalığına bağlı virilizasyon bozukluğu ile seyreden sahip erkek infertilitesi
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Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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Classification

Not placed in any Orphanet classification in this release.

No children.

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Genes

0 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

0 records

No prevalence record in this release.

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HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

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Sources for this card