familial medullary thyroid carcinoma Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050547)
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21 genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
RET ret proto-oncogene 3.1165
CALCA calcitonin-related polypeptide alpha 2.02884
GDNF glial cell derived neurotrophic factor 1.10973
MEN1 multiple endocrine neoplasia I 0.886799
HNRNPA3 heterogeneous nuclear ribonucleoprotein A3 0.742329
LYPD1 LY6/PLAUR domain containing 1 0.683892
PSPN persephin 0.674713
ERC1 ELKS/RAB6-interacting/CAST family member 1 0.6608
PTEN phosphatase and tensin homolog 0.544705
ARTN artemin 0.501909
FRS2 fibroblast growth factor receptor substrate 2 0.385193
YARS tyrosyl-tRNA synthetase 0.334315
NRTN neurturin 0.3292
CSF1 colony stimulating factor 1 (macrophage) 0.242945
GART phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase 0.221108
NTRK1 neurotrophic tyrosine kinase, receptor, type 1 0.217352
GAST gastrin 0.188632
IKBKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta 0.177851
CX3CL1 chemokine (C-X3-C motif) ligand 1 0.168381
ANOS1 anosmin 1 0.167915
MAPK9 mitogen-activated protein kinase 9 0.164786