46,XX disorder of sex development-anorectal anomalies syndrome

46,XX disorder of sex development-anorectal anomalies syndrome is a rare developmental defect during embryogenesis syndrome characterized by a normal female karyotype, normal ovaries, male or ambiguous genitalia, urinary tract malformations (ranging from bilateral renal agenesis to mild unilateral hydronephrosis), Müllerian duct anomalies (e.g. complete absence of the uterus and vagina, bicornuate uterus), and imperforate anus. Additional features may include tracheoesophageal fistula, radial aplasia, and malrotation of the gut.



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症例報告を絞り込む



合計: 0 (症例報告)

  


(表示件数)
対応する徴候・症状  遺伝子  変異  キーワード(MeSH)
順位
(類似度)
PMID
(PMCID)
        

徴候・症状リスト(Orphanetデータベースから取得)

    合計: 15

HPO ID 徴候・症状 頻度
HP:0000812 内性器異常 Very frequent (99-80%)
HP:0002023 鎖肛 Very frequent (99-80%)
HP:0010458 女性仮性半陰陽 Very frequent (99-80%)
HP:0000003 多嚢胞腎異形成 Frequent (79-30%)
HP:0000072 水尿管症 Frequent (79-30%)
HP:0000126 水腎症 Frequent (79-30%)
HP:0000795 尿道異常 Frequent (79-30%)
HP:0001562 羊水過少 Frequent (79-30%)
HP:0002093 呼吸不全 Frequent (79-30%)
HP:0008678 腎低形成/無形成 Frequent (79-30%)
HP:0002566 腸回転異常 Occasional (29-5%)
HP:0002575 気管食道瘻 Occasional (29-5%)
HP:0006501 橈骨無形成/低形成 Occasional (29-5%)
HP:0100627 外部尿道口位置異常 Occasional (29-5%)
HP:0100779 泌尿生殖洞奇形 Occasional (29-5%)


徴候・症状リスト(症例報告から取得)

    合計: 0

HPO ID 徴候・症状 症例報告数


疾患原因遺伝子リスト(Orphanetデータベースから取得)

    合計: 0

Gene Symbol 遺伝子名 Entrez Gene ID