obsolete_Kallmann syndrome true UMLS:C0162809 OMIM:615270 3.41.0 OMIM:615271 Replaced with Mondo term. OMIM:244200 OMIM:612370 OMIM:615266 OMIM:615267 OMIM:615269 OMIM:614897 orphanet MedDRA:10053142 OMIM:614858 ICD10:E23.0 OMIM:614838 OMIM:614837 OMIM:610628 OMIM:147950 OMIM:618841 OMIM:616030 http://purl.obolibrary.org/obo/MONDO_0018800 Congenital hypogonadotropic hypogonadism with anosmia OMIM:614880 OMIM:614840 Olfacto-genital pathological sequence 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). MESH:D017436 OMIM:612702 OMIM:308700