Leydig cell agenesis
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Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
Leydig cell hypoplasia due to complete LH receptor inactivation
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.
agenesie van Leydig-cel door volledige inactivatie van receptor van luteïniserend hormoon
leydigcelhypoplasie door volledige inactivatie van receptor van luteïniserend hormoon
leydigcelhypoplasie door volledige inactivatie van LH-receptor
Id1003437009
StatusPrimitive
Associated morphologyHypoplasia
Finding siteStructure of interstitial cell of Leydig
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
TargetQ56.1
RuleTRUE
AdviceALWAYS Q56.1
CorrelationSNOMED CT source code to target map code correlation not specified