Familial male-limited precocious puberty

Property	Value
rdf:type	owl:NamedIndividual Autosomal dominant disorder Intersex variation Rare disease Congenital disorder Cell surface receptor deficiency
rdfs:label	Familial male-limited precocious puberty
owl:sameAs	dbr:Familial_male-limited_precocious_puberty
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Congenital_disorders http://en.wikipedia.org/wiki/Category:Autosomal_dominant_disorders http://en.wikipedia.org/wiki/Category:Intersex_variations http://en.wikipedia.org/wiki/Category:Rare_diseases http://en.wikipedia.org/wiki/Precocious_puberty http://en.wikipedia.org/wiki/List_of_congenital_disorders http://en.wikipedia.org/wiki/Category:Cell_surface_receptor_deficiencies
skos:prefLabel	Familial male-limited precocious puberty
skos:altLabel	Luteinizing hormone (LH) oversensitivity familial male-limited precocious puberty
clgo:icd10	E30.1
clgo:meshId	C536961
clgo:omim	176410
clgo:orpha	3000

About: clgr:Familial_male-limited_precocious_puberty