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CCND3 3' Untranslated Region Deletion Mutation
The loss of one or more nucleotides encoding the 3'' untranslated region of the CCND3 gene. [from NCI]
CCND1 3' Untranslated Region Deletion Mutation
The loss of one or more nucleotides encoding the 3'' untranslated region of the CCND1 gene. [from NCI]
CCND2 3' Untranslated Region Deletion Mutation
The loss of one or more nucleotides encoding the 3'' untranslated region of the CCND2 gene. [from NCI]
3,3'-diiodothyronine level above reference range
3,3'-diiodothyronine level below reference range
Abnormal 3,3' diiodothyronine
3',5'-cyclic-nucleotide phosphodiesterase inhibitor
3,3'-diiodothyronine within reference range
DIS3 Gene Mutation
A change in the nucleotide sequence of the DIS3 gene. [from NCI]
FIP1L1-PDGFRalpha Fusion Protein Expression
Expression of a fusion protein involving the human genes FIP1L1 and PDGFRA. It results from an inversion or translocation and is associated with hypereosinophilic syndrome (HES)/chronic eosinophilic leukemia (CEL) and systemic mast cell disease. [from NCI]
Deficiency of phosphoadenylate 3'-nucleotidase
Deficiency of 3'-nucleotidase
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