Hirschsprung disease-type D brachydactyly syndrome

Hirschsprung disease-type D brachydactyly syndrome is characterized by Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two maternal uncles). Transmission appears to be X-linked recessive but autosomal dominant inheritance with incomplete penetrance in females can not be ruled out.



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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: 6

HPO ID 徴候・症状 頻度
HP:0002251 無神経節性巨大結腸 Very frequent (99-80%)
HP:0010624 趾爪無形成/低形成 Very frequent (99-80%)
HP:0001156 短指症候群 Frequent (79-30%)
HP:0001804 指爪低形成 Frequent (79-30%)
HP:0009650 短い母指末節骨 Frequent (79-30%)
HP:0010111 短い母趾趾骨 Frequent (79-30%)


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