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About:
clgo:
Intersex_variation
Property
Value
rdf:
type
owl:
Class
rdfs:
label
Intersex variation
rdfs:
subClassOf
Disease
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Category:Intersex_variations
is
rdf:
type
of
Barber–Say syndrome
Cytochrome P450 oxidoreductase deficiency
Partial androgen insensitivity syndrome
45,X/46,XY mosaicism
Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
XXXXY syndrome
Prader–Willi syndrome
Delayed puberty
Hypoestrogenism
Anabolic steroid-induced hypogonadism
Ovotestis
Isolated 17,20-lyase deficiency
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Micropenis
Cytochrome b5 deficiency
Inborn errors of steroid metabolism
Opitz G/BBB syndrome
Polyorchidism
Gonadotropin insensitivity
Cryptorchidism
True hermaphroditism
Klinefelter syndrome
Aromatase deficiency
Seaver Cassidy syndrome
Aarskog–Scott syndrome
17β-Hydroxysteroid dehydrogenase III deficiency
Turner syndrome
Complete androgen insensitivity syndrome
Precocious puberty
Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency
SCARF syndrome
Ablepharon macrostomia syndrome
Bifid penis
Androgen deficiency
Congenital adrenal hyperplasia
Hypospadias
SERKAL syndrome
Hyperestrogenism
Hypogonadism
Aromatase excess syndrome
XY gonadal dysgenesis
Pseudohermaphroditism
Hemochromatosis
Hyperandrogenism
XXXY syndrome
CHARGE syndrome
Diphallia
Clitoromegaly
Leydig cell hypoplasia
Ovotesticular disorder
Penoscrotal transposition
Swyer–James syndrome
Androgen insensitivity syndrome
Hypergonadotropic hypergonadism
Poland syndrome
Androgen-induced hermaphroditism
Progestin-induced virilization
Late onset congenital adrenal hyperplasia
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Denys–Drash syndrome
Familial male-limited precocious puberty
Aphallia
Cloacal exstrophy
Mild androgen insensitivity syndrome
Campomelic dysplasia
Kallmann syndrome
Hypergonadism
MDP syndrome
Müllerian agenesis
Uterus didelphys
5α-Reductase 2 deficiency
XXYY syndrome
Hypogonadotropic hypogonadism
Estrogen insensitivity syndrome
XX male syndrome
Lipoid congenital adrenal hyperplasia
Pseudovaginal perineoscrotal hypospadias
Gonadal dysgenesis
Anorchia
Ring chromosome 18
46,XX/46,XY
Persistent Müllerian duct syndrome
WNT4 deficiency
Opioid Induced Androgen Deficiency