indeterminate leprosy Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A leprosy that is an early form of the disease which causes one to a few hypopigmented or erythematous macules. (Human Disease Ontology, DOID_11851)
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Genes

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

Symbol Name Standardized Value
MLLT1 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 1 1.07152
DEFB1 defensin, beta 1 0.801564
SLC17A5 solute carrier family 17 (acidic sugar transporter), member 5 0.625711
HLA-E major histocompatibility complex, class I, E 0.53928
C4A complement component 4A (Rodgers blood group) 0.522273
MICA MHC class I polypeptide-related sequence A 0.51842
CD68 CD68 molecule 0.418768
NPS neuropeptide S 0.181222