Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Empty Sella Syndrome	[NCBI]

Gene	Link	Information Gain
PRL	[NCBI]	9.73381e-05
TRH	[NCBI]	3.88482e-05
VSX1	[NCBI]	2.65731e-05
AVP	[NCBI]	1.12624e-05
EVI1	[NCBI]	8.27268e-06
TPO	[NCBI]	6.41721e-06

OMIM	Link	Information gain
lateral meningocele syndrome	[NCBI]	0.00119841
PRL	[NCBI]	0.000352203
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant	[NCBI]	0.000106098
VSX1	[NCBI]	7.01659e-05
BBS	[NCBI]	6.97572e-05
GHRL	[NCBI]	4.74381e-05
PWS	[NCBI]	4.28894e-05
SERPINA6	[NCBI]	3.33066e-05
AVP	[NCBI]	2.63506e-05
TPO	[NCBI]	2.30196e-05
CRH	[NCBI]	8.66483e-06
SLE	[NCBI]	4.10457e-06