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MeSH keywords -> Related genes, diseases (OMIM)


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01 Empty Sella Syndrome [NCBI]


Gene


Gene Link Information
Gain
01
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


OMIM Link Information
gain
01
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




Database Center for Life Science