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- XX_gonadal_dysgenesis abstract "This syndrome is inherited as an autosomal disease. It affects both males and females but the phenotype differs. In both sexes sensorineural deafness occurs but in females ovarian dysgenesis also occurs. XX gonadal dysgenesis is a type of female hypogonadism in which no functional ovaries are present to induce puberty in an otherwise normal girl whose karyotype is found to be 46,XX. With nonfunctional streak ovaries she is low in estrogen levels (hypoestrogenic) and has high levels of FSH and LH. Estrogen and progesterone therapy is usually then commenced.".
- XX_gonadal_dysgenesis meshId "D023961".
- XX_gonadal_dysgenesis omim "233300".
- XX_gonadal_dysgenesis wikiPageID "5680651".
- XX_gonadal_dysgenesis wikiPageRevisionID "580144925".
- XX_gonadal_dysgenesis hasPhotoCollection XX_gonadal_dysgenesis.
- XX_gonadal_dysgenesis meshid "D023961".
- XX_gonadal_dysgenesis name "XX gonadal dysgenesis".
- XX_gonadal_dysgenesis omim "233300".
- XX_gonadal_dysgenesis omimMult "Perrault syndrome".
- XX_gonadal_dysgenesis omimMult "XX gonadal dysgenesis".
- XX_gonadal_dysgenesis wordnet_type synset-disease-noun-1.
- XX_gonadal_dysgenesis subject Category:Cell_surface_receptor_deficiencies.
- XX_gonadal_dysgenesis subject Category:Gynaecologic_disorder.
- XX_gonadal_dysgenesis type Abstraction100002137.
- XX_gonadal_dysgenesis type Attribute100024264.
- XX_gonadal_dysgenesis type CellSurfaceReceptorDeficiencies.
- XX_gonadal_dysgenesis type Condition113920835.
- XX_gonadal_dysgenesis type Disease114070360.
- XX_gonadal_dysgenesis type IllHealth114052046.
- XX_gonadal_dysgenesis type Illness114061805.
- XX_gonadal_dysgenesis type Lack114449405.
- XX_gonadal_dysgenesis type Need114449126.
- XX_gonadal_dysgenesis type PathologicalState114051917.
- XX_gonadal_dysgenesis type PhysicalCondition114034177.
- XX_gonadal_dysgenesis type State100024720.
- XX_gonadal_dysgenesis type Disease.
- XX_gonadal_dysgenesis type AilmentCondition.
- XX_gonadal_dysgenesis type Situation.
- XX_gonadal_dysgenesis comment "This syndrome is inherited as an autosomal disease. It affects both males and females but the phenotype differs. In both sexes sensorineural deafness occurs but in females ovarian dysgenesis also occurs. XX gonadal dysgenesis is a type of female hypogonadism in which no functional ovaries are present to induce puberty in an otherwise normal girl whose karyotype is found to be 46,XX.".
- XX_gonadal_dysgenesis label "XX gonadal dysgenesis".
- XX_gonadal_dysgenesis sameAs m.0dztwr.
- XX_gonadal_dysgenesis sameAs Q8042656.
- XX_gonadal_dysgenesis sameAs Q8042656.
- XX_gonadal_dysgenesis sameAs 2516.
- XX_gonadal_dysgenesis sameAs XX_gonadal_dysgenesis.
- XX_gonadal_dysgenesis wasDerivedFrom XX_gonadal_dysgenesis?oldid=580144925.
- XX_gonadal_dysgenesis isPrimaryTopicOf XX_gonadal_dysgenesis.
- XX_gonadal_dysgenesis name "XX gonadal dysgenesis".