multiple symmetric lipomatosis 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_14116)
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12 genes co-occuring with the disease multiple symmetric lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
UCP1 uncoupling protein 1 (mitochondrial, proton carrier) 1.26255
ACP1 acid phosphatase 1, soluble 1.09797
LIPE lipase, hormone-sensitive 0.846669
SCD stearoyl-CoA desaturase (delta-9-desaturase) 0.802385
POLG polymerase (DNA directed), gamma 0.751678
LPL lipoprotein lipase 0.408292
MEN1 multiple endocrine neoplasia I 0.408292
LPA lipoprotein, Lp(a) 0.332487
TRH thyrotropin-releasing hormone 0.283297
PRL prolactin 0.235964
PPARG peroxisome proliferator-activated receptor gamma 0.235616
HLA-C major histocompatibility complex, class I, C 0.200656