disease has feature Infertility Osteoporosis syndromic disease hypogonadotropic hypogonadism Kallmann syndrome https://www.malacards.org/card/kallmann_syndrome Olfacto-genital pathological sequence DOID:3614 MESH:D017436 Kallmann syndrome (KS) is a developmental genetic disorder characterized by the association of congenital hypogonadotropic hypogonadism (CHH) due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs). MONDO:0018800 congenital hypogonadotropic hypogonadism with anosmia Orphanet:478 UMLS:C0162809 NCIT:C75479 NORD:1319 MEDGEN:102469 MedDRA:10053142 GARD:0010771 NANDO:2200381 SCTID:93559003 hypogonadotropic hypogonadism with anosmia ICD9:253.4