Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Exophthalmos	[NCBI]

Gene	Link	Information Gain
PRL	[NCBI]	1.86595e-05
CD68	[NCBI]	1.30251e-05
XCL1	[NCBI]	1.14023e-05
CD52	[NCBI]	8.82969e-06
PAX3	[NCBI]	8.30369e-06
FOXO1	[NCBI]	8.24625e-06
CD99	[NCBI]	7.87919e-06
TRH	[NCBI]	5.78787e-06
ACHE	[NCBI]	5.40614e-06
AFP	[NCBI]	4.36229e-06

OMIM	Link	Information gain
CMDR	[NCBI]	0.000840405
robinow syndrome, autosomal dominant	[NCBI]	0.000676229
NLS	[NCBI]	0.000626005
RNS	[NCBI]	0.000438008
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features	[NCBI]	0.000109365
microcephaly, corpus callosum dysgenesis, and cleft lip/palate	[NCBI]	0.000109365
acrofrontofacionasal dysostosis, severe	[NCBI]	0.000109365
PRL	[NCBI]	9.65776e-05
desmosterolosis	[NCBI]	9.65043e-05
GRTH	[NCBI]	9.14716e-05
ABS	[NCBI]	6.93203e-05
graves disease	[NCBI]	6.72698e-05
RBS	[NCBI]	6.54521e-05
CRMO	[NCBI]	5.67342e-05
MG	[NCBI]	3.7561e-05
ACHE	[NCBI]	2.48822e-05
AFP	[NCBI]	1.9185e-05
RA	[NCBI]	1.1009e-05
SLE	[NCBI]	4.85239e-06