3 Matching Annotations
  1. Apr 2022
    1. Pathogenic germline variants in DICER1 underlie an autosomal dominant, pleiotropic tumor-predisposition disorder.

      gene name: DICER1 PMID: 33570641 HGNCID: none inheritance pattern: autosomal dominant disease entity: benign and malignant tumors mutation: germline zygosity: heterozygous variant: none family information: none

    1. PMID: 34599283

      pub med ID

    2. DICER1 syndrome (OMIM 606241, 601200) is a rare autosomal dominant familial tumor predisposition disorder with a heterozygous DICER1 germline mutation.

      autosomal dominant disorder