FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

33927004: Hypogonadotropic hypogonadism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
56637011 Hypogonadotropic hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
56639014 Secondary hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
485671015 Gonadotrophin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
765389014 Hypogonadotropic hypogonadism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
56637011 Hypogonadotropic hypogonadism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
56637011 Hypogonadotropic hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
56639014 Secondary hypogonadism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
56639014 Secondary hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
485671015 Gonadotrophin deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
485671015 Gonadotrophin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
765389014 Hypogonadotropic hypogonadism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
765389014 Hypogonadotropic hypogonadism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
591371000172112 hypogonadisme hypogonadotrope fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
591371000172112 hypogonadisme hypogonadotrope fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


35 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypogonadotropic hypogonadism Is a Hypogonadism (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism Is a Hypopituitarism true Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism Finding site Pars anterior of pituitary gland false Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism Finding site Gonadal endocrine structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypogonadotropic hypogonadism Is a Disorder of anterior pituitary true Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism Finding site Structure of distal part of pituitary true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Isolated gonadotropin deficiency Is a False Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Follicle stimulating hormone deficiency Is a False Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
LH - luteinising hormone deficiency Is a False Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic hypogonadotropic hypogonadism Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Female hypogonadotropic hypogonadism Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Adiposogenital dystrophy (disorder) Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadism with anosmia Is a False Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism due to luteinising hormone deficiency Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency (disorder) Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
This syndrome is characterized by the association of hypogonadotropic hypogonadism and frontoparietal alopecia. Is a False Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) Is a False Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
This syndrome is characterized by the association of intellectual deficit, congenital cataract, and hypogonadotropic hypogonadism. Is a False Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypogonadotropic hypogonadism (disorder) Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Functional hypogonadotropic hypogonadism (disorder) Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Boucher Neuhäuser syndrome Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
Progressive cerebellar ataxia with hypogonadism Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
4H leucodystrophy Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic disease characterized by childhood onset of multiple endocrine manifestations in combination with central and peripheral nervous system abnormalities. Reported signs and symptoms include postnatal growth retardation, moderate intellectual disability, hypogonadotropic hypogonadism, insulin-dependent diabetes mellitus, central hypothyroidism, demyelinating sensorimotor polyneuropathy, and cerebellar and pyramidal signs. Progressive hearing loss and a hypoplastic pituitary gland have also been described. Brain imaging shows moderate white matter abnormalities. Is a True Hypogonadotropic hypogonadism Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start