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hypogonadotropic hypogonadism 24 without anosmia

MeSH: C537070ORPHA: 52901

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

hypogonadotropic hypogonadism that has material basis in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with hypogonadotropic hypogonadism 24 without anosmia, sourced from HPO and Orphanet clinical annotations.

Male hypogonadismFemale hypogonadismGonadotropin deficiencyHypogonadotropic hypogonadismPrimary amenorrheaDelayed pubertySparse axillary hairSparse pubic hairDelayed skeletal maturationDecreased serum estradiolDecreased testicular sizeDelayed menarcheDecreased serum testosterone concentrationAzoospermiaTesticular atrophyOligozoospermiaOligomenorrheaHyperplasia of the Leydig cellsBilateral breast hypoplasiaAbnormal sperm morphologyDecreased female libido

Classification & Codes

MeSH Code

C537070

Orphanet Code

ORPHA:52901
hypogonadotropic hypogonadism 24 without anosmia
MeSHC537070
OrphanetORPHA:52901
Treatments0 drug(s)
Symptoms on record21 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO