Isolated FSH deficiency (Q97196): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Created a new Item
 
‎Changed an Item
 
(6 intermediate revisions by the same user not shown)
description / pt-brdescription / pt-br
 
Transtorno raro de comprometimento da síntese/secreção do hormônio folículo-estimulante (FSH) pela glândula pituitária, manifestando-se com hipogonadismo hipogonadotrófico, usualmente causado por uma mutação no gene da subunidade beta do FSH.
description / endescription / en
 
A rare disorder of impaired synthesis/secretion of follicle-stimulating hormone (FSH) in the pituitary gland, manifesting in hypogonadotropic hypogonadism, usually caused by a mutation of FSH beta subunit gene.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1431378723 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_1431378723
Property / CURIE: CID11:ID_1431378723 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_1431378723
Property / Canary Token: dki-india-ID_1431378723 / rank
 
Normal rank
Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank
Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
Normal rank
Property / Collection date
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
Normal rank

Latest revision as of 13:14, 16 August 2026

A rare disorder of impaired synthesis/secretion of follicle-stimulating hormone (FSH) in the pituitary gland, manifesting in hypogonadotropic hypogonadism, usually caused by a mutation of FSH beta subunit gene.
Language Label Description Also known as
default for all languages
ID_1431378723
    English
    Isolated FSH deficiency
    A rare disorder of impaired synthesis/secretion of follicle-stimulating hormone (FSH) in the pituitary gland, manifesting in hypogonadotropic hypogonadism, usually caused by a mutation of FSH beta subunit gene.

      Statements

      CID11:ID_1431378723
      0 references
      dki-india-ID_1431378723
      0 references
      Concluído
      0 references
      15 August 2026
      0 references