has material basis in germline mutation in LHB hypogonadotropic hypogonadism 23 with or without anosmia https://www.malacards.org/card/hypogonadotropic_hypogonadism_23_with_or_without_anosmia SCTID:8829008 LHB hypogonadotropic hypogonadism hypogonadotropic hypogonadism 23 without anosmia ICD9:253.4 DOID:0090091 46,XY DSD due to LHB deficiency MESH:C537919 46,XY disorder of sex development due to LHB deficiency Pasqualini syndrome Leydig cell hypoplasia due to LHB deficiency eunuchoidism with spermatogenesis, normal FSH and low or normal interstitial cell-stimulating hormone (ICSH) UMLS:C0271582 46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency fertile eunuch syndrome OMIM:228300 MEDGEN:82881 HH23 MONDO:0009223 Orphanet:325448 hypogonadotropic hypogonadism caused by mutation in LHB GARD:0010127 Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the LHB gene. 46,XY DSD due to luteinizing hormone subunit beta deficiency hypogonadotropic hypogonadism Leydig cell hypoplasia