About: Intersex variations

An Entity of Type: Concept, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Property	Value
dbo:wikiPageID	62057204 (xsd:integer)
dbo:wikiPageRevisionID	1018444628 (xsd:integer)
rdf:type	skos:Concept
rdfs:label	Intersex variations (en)
skos:broader	dbc:Intersex_and_medicine dbc:Medicine dbc:Rare_diseases
skos:prefLabel	Intersex variations (en)
prov:wasDerivedFrom	wikipedia-en:Category:Intersex_variations?oldid=1018444628&ns=14
is dbo:wikiPageWikiLink of	dbr:Prader–Willi_syndrome dbr:Persistent_Müllerian_duct_syndrome dbr:Progestin-induced_virilization dbr:Androgen-induced_hermaphroditism dbr:Androgen_deficiency dbr:Anorchia dbr:Aphallia dbr:Hyperandrogenism dbr:Hypospadias dbr:Cytochrome_P450_oxidoreductase_deficiency dbr:Cytochrome_b5_deficiency dbr:Delayed_puberty dbr:Inborn_errors_of_steroid_metabolism dbr:Leydig_cell_hypoplasia dbr:Pseudohermaphroditism dbr:XXYY_syndrome dbr:Complete_androgen_insensitivity_syndrome dbr:Cryptorchidism dbr:Seaver_Cassidy_syndrome dbr:17β-Hydroxysteroid_dehydrogenase_III_deficiency dbr:Congenital_adrenal_hyperplasia dbr:Congenital_adrenal_hyperplasia_due_to_11β-hydroxylase_deficiency dbr:Congenital_adrenal_hyperplasia_due_to_17α-hydroxylase_deficiency dbr:Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency dbr:Congenital_adrenal_hyperplasia_due_to_3β-hydroxysteroid_dehydrogenase_deficiency dbr:True_hermaphroditism dbr:Opitz_G/BBB_syndrome dbr:Androgen_insensitivity_syndrome dbr:Aromatase_deficiency dbr:Aromatase_excess_syndrome dbr:Clitoromegaly dbr:Cloacal_exstrophy dbr:Denys–Drash_syndrome dbr:Poland_syndrome dbr:5α-Reductase_2_deficiency dbr:Turner_syndrome dbr:Late_onset_congenital_adrenal_hyperplasia dbr:Lipoid_congenital_adrenal_hyperplasia dbr:Micropenis dbr:SCARF_syndrome dbr:46,XX/46,XY dbr:45,X/46,XY_mosaicism dbr:Barber–Say_syndrome dbr:Partial_androgen_insensitivity_syndrome dbr:Diphallia dbr:Familial_male-limited_precocious_puberty dbr:Gonadal_dysgenesis dbr:Gonadotropin_insensitivity dbr:Isolated_17,20-lyase_deficiency dbr:Precocious_puberty dbr:Hyperestrogenism dbr:Hypergonadism dbr:Hypergonadotropic_hypergonadism dbr:Hypoestrogenism dbr:Hypogonadism dbr:Hypogonadotropic_hypogonadism dbr:Aarskog–Scott_syndrome dbr:Ablepharon_macrostomia_syndrome dbr:Kallmann_syndrome dbr:Bifid_penis dbr:Penoscrotal_transposition dbr:XXXY_syndrome dbr:CHARGE_syndrome dbr:Klinefelter_syndrome dbr:Mild_androgen_insensitivity_syndrome dbr:Campomelic_dysplasia dbr:XX_male_syndrome dbr:MDP_syndrome dbr:Estrogen_insensitivity_syndrome dbr:Uterus_didelphys dbr:Ovotestis dbr:Müllerian_agenesis dbr:Polyorchidism dbr:XY_gonadal_dysgenesis dbr:SERKAL_syndrome dbr:WNT4_deficiency dbr:Ring_chromosome_18 dbr:XXXXY_syndrome
is dcterms:subject of	dbr:Prader–Willi_syndrome dbr:Persistent_Müllerian_duct_syndrome dbr:Progestin-induced_virilization dbr:Androgen-induced_hermaphroditism dbr:Androgen_deficiency dbr:Anorchia dbr:Aphallia dbr:Hyperandrogenism dbr:Hypospadias dbr:Cytochrome_P450_oxidoreductase_deficiency dbr:Cytochrome_b5_deficiency dbr:Delayed_puberty dbr:Inborn_errors_of_steroid_metabolism dbr:Leydig_cell_hypoplasia dbr:Pseudohermaphroditism dbr:XXYY_syndrome dbr:Complete_androgen_insensitivity_syndrome dbr:Cryptorchidism dbr:Seaver_Cassidy_syndrome dbr:17β-Hydroxysteroid_dehydrogenase_III_deficiency dbr:Congenital_adrenal_hyperplasia dbr:Congenital_adrenal_hyperplasia_due_to_11β-hydroxylase_deficiency dbr:Congenital_adrenal_hyperplasia_due_to_17α-hydroxylase_deficiency dbr:Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency dbr:Congenital_adrenal_hyperplasia_due_to_3β-hydroxysteroid_dehydrogenase_deficiency dbr:True_hermaphroditism dbr:Opitz_G/BBB_syndrome dbr:Androgen_insensitivity_syndrome dbr:Aromatase_deficiency dbr:Aromatase_excess_syndrome dbr:Clitoromegaly dbr:Cloacal_exstrophy dbr:Denys–Drash_syndrome dbr:Poland_syndrome dbr:5α-Reductase_2_deficiency dbr:Turner_syndrome dbr:Late_onset_congenital_adrenal_hyperplasia dbr:Lipoid_congenital_adrenal_hyperplasia dbr:Micropenis dbr:SCARF_syndrome dbr:46,XX/46,XY dbr:45,X/46,XY_mosaicism dbr:Barber–Say_syndrome dbr:Partial_androgen_insensitivity_syndrome dbr:Diphallia dbr:Familial_male-limited_precocious_puberty dbr:Gonadal_dysgenesis dbr:Gonadotropin_insensitivity dbr:Isolated_17,20-lyase_deficiency dbr:Precocious_puberty dbr:Hyperestrogenism dbr:Hypergonadism dbr:Hypergonadotropic_hypergonadism dbr:Hypoestrogenism dbr:Hypogonadism dbr:Hypogonadotropic_hypogonadism dbr:Aarskog–Scott_syndrome dbr:Ablepharon_macrostomia_syndrome dbr:Kallmann_syndrome dbr:Bifid_penis dbr:Penoscrotal_transposition dbr:XXXY_syndrome dbr:CHARGE_syndrome dbr:Klinefelter_syndrome dbr:Mild_androgen_insensitivity_syndrome dbr:Campomelic_dysplasia dbr:XX_male_syndrome dbr:MDP_syndrome dbr:Estrogen_insensitivity_syndrome dbr:Uterus_didelphys dbr:Ovotestis dbr:Müllerian_agenesis dbr:Polyorchidism dbr:XY_gonadal_dysgenesis dbr:SERKAL_syndrome dbr:WNT4_deficiency dbr:Ring_chromosome_18 dbr:XXXXY_syndrome