hypogonadotropic hypogonadism 23 with or without anosmia
MeSH: C537919ORPHA: 325448
Overview
hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C537919Orphanet Code
ORPHA:325448hypogonadotropic hypogonadism 23 with or without anosmia
| MeSH | C537919 |
| Orphanet | ORPHA:325448 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO