Dahlberg-Borer-Newcomer syndrome

Dahlberg-Borer-Newcomer syndrome is a very rare ectodermal dysplasia syndrome, described in 2 adult brothers, characterized by the association of hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hyperthricoses, and nail abnormalities.



患者の 徴候症状 を入力


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: 17

HPO ID 徴候・症状 頻度
HP:0000112 腎症 Very frequent (99-80%)
HP:0000431 幅広い鼻梁 Very frequent (99-80%)
HP:0000506 内眼角外方偏位 Very frequent (99-80%)
HP:0000821 甲状腺機能低下症 Very frequent (99-80%)
HP:0000829 副甲状腺機能低下症 Very frequent (99-80%)
HP:0000966 減汗症 Very frequent (99-80%)
HP:0001004 リンパ性浮腫 Very frequent (99-80%)
HP:0001072 分厚い皮膚 Very frequent (99-80%)
HP:0001156 短指症候群 Very frequent (99-80%)
HP:0001634 僧帽弁逸脱 Very frequent (99-80%)
HP:0001798 無爪症 Very frequent (99-80%)
HP:0002230 全身性多毛 Very frequent (99-80%)
HP:0002901 低カルシウム血症 Very frequent (99-80%)
HP:0004322 低身長 Very frequent (99-80%)
HP:0009882 短い指末節骨 Very frequent (99-80%)
HP:0000518 白内障 Frequent (79-30%)
HP:0000083 腎不全 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