3 Matching Annotations
- Apr 2022
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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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
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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PMID: 34599283
pub med ID
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DICER1 syndrome (OMIM 606241, 601200) is a rare autosomal dominant familial tumor predisposition disorder with a heterozygous DICER1 germline mutation.
autosomal dominant disorder
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