Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Kallmans syndrom hos kvinde | Is a | False | Hypogonadism with anosmia | Inferred relationship | Some | |
Kallmann syndrome with cardiopathy is characterized by hypogonadotropic hypogonadism associated with gonadotropin-releasing hormone (GnRH) deficiency, anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs) and complex congenital cardiac malformations (double-outlet right ventricle, dilated cardiomyopathy, right aortic arch). It represents a distinct clinical entity from Kallmann syndrome. | Is a | True | Hypogonadism with anosmia | Inferred relationship | Some | |
Amenorrhea due to congenital gonadotrophin releasing hormone deficiency | Due to | True | Hypogonadism with anosmia | Inferred relationship | Some | 3 |
This concept is not in any reference sets