laurence-moon syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_1930)
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Genes

8 genes co-occuring with the disease laurence-moon syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PDXP pyridoxal (pyridoxine, vitamin B6) phosphatase 1.31275
MKKS McKusick-Kaufman syndrome 1.21695
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1 1.18496
NID1 nidogen 1 1.03746
RPGR retinitis pigmentosa GTPase regulator 0.954108
RARA retinoic acid receptor, alpha 0.658818
TRH thyrotropin-releasing hormone 0.385936
FN1 fibronectin 1 0.219398