- May 2022
-
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
-
DICER1 syndrome is a rare genetic condition predisposing to hereditary cancer and caused by variants in the DICER1
GeneName: DICER1 PMCID: PMC7859642 HGNCID: Unavailable Inheritance Pattern: Autosomal dominant. Disease Entity: Familial pleuropulmonary blastoma (PPB), cervix embryonal rhabdomyosarcoma, multinodular goiter, nasal chondromesenchymal hemartoma, Ciliary body medulloepithelioma, Sertoli-Leydig Cell Tumor (SLCT), differentiated thyroid carcinoma, pituitary blastoma, pineoblastoma, cystic nephroma, Wilm's tumor and sarcomas of different sites including, amongst others, the uterine cervix, kidney and brain. Mutation: Germline Zygosity: Heterozygose Variant: No ClinVarID present. Family Information: No family outline Case: No specified information of patients included. CasePresentingHPO's: n/a CasePrevious Testing: n/a gnomAD: n/a Mutation Type: nonsense, frameshift, or splice affected.
Tags
- Mutation type: Frameshift
- Gene: DICER1
- Multinodular goiter
- Zygosity: Heterozygous
- Ciliary body medulloepitheliomma
- Inheritance Pattern: Autosomal dominant
- Differentiated thyroid carcinoma
- Mutation type: Nonsense
- Mutation: Germline
- Wilm's tumor
- PMCID: PMC7859642
- Sertoli-Letdig Cell Tumor(SLCT)
- Nasal chondromesenchymal hemartoma
- Familial pleuropulmonary blastoma (PPB)
- Cervix embryonal rhabdomyosarcoma
Annotators
URL
-