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hypogonadotropic hypogonadism 12 with or without anosmia

MeSH: C535764ORPHA: 1958

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21

Available Treatments (0)

No treatments linked yet

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

Classification & Codes

MeSH Code

C535764

Orphanet Code

ORPHA:1958
hypogonadotropic hypogonadism 12 with or without anosmia
MeSHC535764
OrphanetORPHA:1958
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
hypogonadotropic hypogonadism 12 with or without anosmia | OrphanDrug