Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Inbreeding [NCBI]

Gene


 Gene Link Information
Gain		 01
DBQD [NCBI] 0.000163802
UOX [NCBI] 0.000119737
MS [NCBI] 1.62998e-05
ZNRF4 [NCBI] 4.11521e-06
ESR1 [NCBI] 3.62796e-06
PRMT7 [NCBI] 3.53459e-06
DYM [NCBI] 3.43668e-06
TRPM1 [NCBI] 3.43668e-06
TMC1 [NCBI] 3.30946e-06
PDE7A [NCBI] 3.2671e-06
MMP11 [NCBI] 3.21016e-06
TRO [NCBI] 3.07265e-06
PDE3B [NCBI] 2.98862e-06
BRMS1 [NCBI] 2.98862e-06
LYST [NCBI] 2.96721e-06
ATP2A1 [NCBI] 2.90845e-06
S1PR1 [NCBI] 2.85642e-06
ATP2C1 [NCBI] 2.83248e-06
NKX3-1 [NCBI] 2.78809e-06
AHSG [NCBI] 2.7742e-06
MSR1 [NCBI] 2.64944e-06
NCAN [NCBI] 2.63412e-06
HBG2 [NCBI] 2.55168e-06
TPP1 [NCBI] 2.47836e-06
CNTN1 [NCBI] 2.44406e-06
CLN3 [NCBI] 2.42783e-06
CNTN2 [NCBI] 2.35714e-06
CSTB [NCBI] 2.35442e-06
MST1R [NCBI] 2.31797e-06
MSH3 [NCBI] 2.24214e-06
CASR [NCBI] 2.17175e-06
WFDC5 [NCBI] 2.16634e-06
ADAR [NCBI] 2.09224e-06
AREG [NCBI] 2.05299e-06
CBX4 [NCBI] 2.02597e-06
JAK3 [NCBI] 1.93592e-06
KRAS [NCBI] 1.86732e-06
PKD1 [NCBI] 1.85192e-06
FGFR3 [NCBI] 1.79587e-06
ATM [NCBI] 1.78807e-06
TGFBR1 [NCBI] 1.69427e-06
ACE [NCBI] 1.44394e-06
VDR [NCBI] 1.33457e-06
NOS2 [NCBI] 1.26717e-06
AVP [NCBI] 1.06897e-06
BDNF [NCBI] 1.06837e-06
ACHE [NCBI] 1.02563e-06
PTH [NCBI] 8.82641e-07
PRL [NCBI] 8.51478e-07



OMIM


 OMIM Link Information
gain		 01
hairy elbows [NCBI] 0.00105558
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000799687
mesothelioma, malignant [NCBI] 0.000747451
hashimoto thyroiditis [NCBI] 0.000635982
pena-shokeir syndrome, type i [NCBI] 0.000560945
spondyloepimetaphyseal dysplasia, genevieve type [NCBI] 0.00016457
spastic quadriplegia, retinitis pigmentosa, and mental retardation [NCBI] 0.00016457
NFRCD [NCBI] 0.000136801
clubfoot [NCBI] 0.000119521
nevo syndrome [NCBI] 0.000119521
DFNB7 [NCBI] 0.000110435
ehlers-danlos syndrome, type vii, autosomal recessive [NCBI] 0.000104219
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1 [NCBI] 9.24643e-05
blood group, p system [NCBI] 8.84583e-05
UOX [NCBI] 8.31804e-05
EVC [NCBI] 7.90172e-05
hypophosphatasia, infantile [NCBI] 7.68842e-05
OCA2 [NCBI] 7.37736e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 7.21188e-05
HYPP [NCBI] 7.21188e-05
sotos syndrome [NCBI] 6.87268e-05
glioma of brain, familial [NCBI] 6.74355e-05
krabbe disease [NCBI] 5.39027e-05
DBA [NCBI] 5.34937e-05
TSD [NCBI] 4.07698e-05
MAGEA5 [NCBI] 3.986e-05
PDE7A [NCBI] 3.986e-05
MAGEA8 [NCBI] 3.986e-05
CENPF [NCBI] 3.986e-05
GNG2 [NCBI] 3.986e-05
SOX18 [NCBI] 3.986e-05
TRPM1 [NCBI] 3.61649e-05
amyloidosis vi [NCBI] 3.58063e-05
SIPA1 [NCBI] 3.45679e-05
LAMB1 [NCBI] 3.33111e-05
LYST [NCBI] 3.06253e-05
orotic aciduria i [NCBI] 3.02759e-05
GALC [NCBI] 2.78136e-05
CHM [NCBI] 2.7594e-05
CSTB [NCBI] 2.6789e-05
SCN4A [NCBI] 2.47432e-05
HBG2 [NCBI] 2.41135e-05
RLBP1 [NCBI] 2.35448e-05
PARG [NCBI] 2.32283e-05
FA [NCBI] 2.06506e-05
HEXA [NCBI] 2.04264e-05
CASR [NCBI] 1.71273e-05
SERPINA6 [NCBI] 1.43722e-05
FGFR3 [NCBI] 1.43066e-05
GPI [NCBI] 1.34246e-05
CYP1A1 [NCBI] 1.04635e-05
TLR4 [NCBI] 1.0204e-05
SPP1 [NCBI] 7.47373e-06
G6PD [NCBI] 5.8088e-06
VDR [NCBI] 5.3921e-06
TNFSF6 [NCBI] 5.34199e-06
BDNF [NCBI] 2.1474e-06
EPO [NCBI] 1.8599e-06
AVP [NCBI] 1.47852e-06
ACHE [NCBI] 1.38519e-06
PTH [NCBI] 6.40486e-07
PRL [NCBI] 4.98271e-07



Database Center for Life Science