Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Leydig_cell_hypoplasia> ?p ?o }
- Leydig_cell_hypoplasia wikiPageUsesTemplate Template:Receptor_deficiencies.
- Leydig_cell_hypoplasia wikiPageUsesTemplate Template:Reflist.
- Leydig_cell_hypoplasia wikiPageUsesTemplate coregulator_deficiencies.
- Leydig_cell_hypoplasia subject Category:Autosomal_recessive_disorders.
- Leydig_cell_hypoplasia subject Category:Endocrine_gonad_disorders.
- Leydig_cell_hypoplasia subject Category:Gonadotropin-releasing_hormone_and_gonadotropins.
- Leydig_cell_hypoplasia subject Category:Intersex_and_medicine.
- Leydig_cell_hypoplasia subject Category:Rare_diseases.
- Leydig_cell_hypoplasia subject Category:Syndromes.
- Leydig_cell_hypoplasia hypernym Syndrome.
- Leydig_cell_hypoplasia type Agent.
- Leydig_cell_hypoplasia type Disease.
- Leydig_cell_hypoplasia type Agent.
- Leydig_cell_hypoplasia type Disorder.
- Leydig_cell_hypoplasia type Hormone.
- Leydig_cell_hypoplasia type Syndrome.
- Leydig_cell_hypoplasia comment "Leydig cell hypoplasia (or aplasia) (LCH), also known as Leydig cell agenesis, is a rare autosomal recessive genetic and endocrine syndrome affecting an estimated 1 in 1,000,000 biological males. It is characterized by an inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signaling Leydig cells of the testicles to produce testosterone and other androgen sex hormones.".
- Leydig_cell_hypoplasia label "Leydig cell hypoplasia".
- Leydig_cell_hypoplasia sameAs m.0j_7psr.
- Leydig_cell_hypoplasia sameAs Q6538005.
- Leydig_cell_hypoplasia sameAs Q6538005.
- Leydig_cell_hypoplasia wasDerivedFrom Leydig_cell_hypoplasia?oldid=668120669.
- Leydig_cell_hypoplasia isPrimaryTopicOf Leydig_cell_hypoplasia.