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1003438004: Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder)


Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4168246015 Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation en Synonym Active Case sensitive SNOMED CT core
4168247012 Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation en Synonym Active Case sensitive SNOMED CT core
4168248019 Leydig cell hypoplasia due to partial LH receptor inactivation en Synonym Active Case sensitive SNOMED CT core
4168249010 Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder) en Fully specified name Active Case sensitive SNOMED CT core
4164767014 This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a partial 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 Case sensitive SNOMED CT core
4283399015 This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a partial 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation Is a Leydig cell agenesis true Inferred relationship Some
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation Finding site Structure of interstitial cell of Leydig true Inferred relationship Some 1
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation Occurrence Congenital true Inferred relationship Some 1
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation Pathological process Pathological developmental process true Inferred relationship Some 1
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation Associated morphology Hypoplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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