Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Menopause, Premature [NCBI]

Gene


 Gene Link Information
Gain		 01
FRAXA [NCBI] 0.000474958
FMR1 [NCBI] 8.58449e-05
SHBG [NCBI] 1.923731e-05
POLG [NCBI] 1.190364e-05
STAR [NCBI] 1.174847e-05
TP63 [NCBI] 8.81546e-06
ACP5 [NCBI] 7.98602e-06
BRCA1 [NCBI] 7.20944e-06
VDR [NCBI] 6.93749e-06
PTH [NCBI] 4.18367e-06



OMIM


 OMIM Link Information
gain		 01
MENOQ1 [NCBI] 0.00272397
POF1 [NCBI] 0.000650718
BPES [NCBI] 0.000345977
mullerian aplasia [NCBI] 0.000266515
PEOA4 [NCBI] 0.000258035
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 [NCBI] 0.0002159885
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2 [NCBI] 0.0002134795
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 0.0001979672
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 [NCBI] 0.0001901895
NS1 [NCBI] 0.0001302046
SHBG [NCBI] 0.0001214098
LAM [NCBI] 0.0001106812
POLG [NCBI] 9.31689e-05
ESR1 [NCBI] 8.15184e-05
PTH [NCBI] 2.141724e-05
SLE [NCBI] 3.31277356e-07



Database Center for Life Science