Leydig cell agenesis
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Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder)
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation
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.
agenesie van Leydig-cel door partiële inactivatie van receptor van luteïniserend hormoon
leydigcelhypoplasie door gedeeltelijk inactivatie van LH-receptor
leydigcelhypoplasie door partiële inactivatie van receptor van luteïniserend hormoon
Id1003438004
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