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1003437009: Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4168242018 Leydig cell hypoplasia due to complete LH receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168243011 Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168244017 Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168245016 Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4164764019 This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a complete inability of the body to respond to luteinising hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4283400010 This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a complete inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168242018 Leydig cell hypoplasia due to complete LH receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168243011 Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168244017 Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168245016 Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4164764019 This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a complete inability of the body to respond to luteinising hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4283400010 This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a complete inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
6377761000241113 hypoplasie des cellules de Leydig par inactivation complète du récepteur LH (luteinizing hormone) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6377771000241117 hypoplasie des cellules de Leydig par résistance complète à l'ICSH (interstitial cell stimulating hormone) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6377781000241115 hypoplasie des cellules de Leydig par résistance complète à l'hormone lutéinisante fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6377761000241113 hypoplasie des cellules de Leydig par inactivation complète du récepteur LH (luteinizing hormone) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6377771000241117 hypoplasie des cellules de Leydig par résistance complète à l'ICSH (interstitial cell stimulating hormone) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6377781000241115 hypoplasie des cellules de Leydig par résistance complète à l'hormone lutéinisante fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation Is a Leydig cell agenesis true Inferred relationship Existential restriction modifier (core metadata concept)
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation Finding site Structure of interstitial cell of Leydig true Inferred relationship Existential restriction modifier (core metadata concept) 1
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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