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bn:03376794n
Noun Concept
Categories: Gynaecologic disorders, Cell surface receptor deficiencies
EN
XX gonadal dysgenesis  46 XX gonadal dysgenesis  46 xx gonadal dysgenesis epibulbar dermoid  Bilateral ovarian agenesis  Gonadal Dysgenesis, 20 Type
EN
XX gonadal dysgenesis is a type of female hypogonadism in which the ovaries do not function to induce puberty in an otherwise normal girl whose karyotype is found to be 46,XX. Wikipedia
Definitions
Relations
Sources
EN
XX gonadal dysgenesis is a type of female hypogonadism in which the ovaries do not function to induce puberty in an otherwise normal girl whose karyotype is found to be 46,XX. Wikipedia
Gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female Wikidata
IS A
gonadal dysgenesis
HAS KIND
Perrault syndrome
GENETIC ASSOCIATION
follicle-stimulating hormone receptor
HEALTH SPECIALTY
medical genetics
MEDICAL CONDITION
medical genetics
Wikipedia
EN
XX gonadal dysgenesis
Wikidata
EN
46 XX gonadal dysgenesis
Wikipedia Redirections
EN
46 xx gonadal dysgenesis epibulbar dermoid, Bilateral ovarian agenesis, Gonadal dysgenesis, XX type, Hypergonadotropic ovarian failure, familial or sporadic, Perrault syndrome
Wikidata Alias
EN
Gonadal Dysgenesis, 20 Type, GONADAL DYSGENESIS, XX TYPE, ODG1, ovarian dysgenesis, Ovarian Dysgenesis, Hypergonadotropic, Autosomal Recessive, Ovarian Dysgenesis, Hypergonadotropic, With Normal Karyotype, OVARIAN DYSGENESIS 1; ODG1, OVARIAN FAILURE, HYPERGONADOTROPIC, XX GONADAL DYSGENESIS, XXGD

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