Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ear Ossicles [NCBI]

Gene


 Gene Link Information
Gain		 01
HFM [NCBI] 0.000696015
BMP2 [NCBI] 9.2194e-06
DLX6 [NCBI] 8.19012e-06
FLNA [NCBI] 6.27529e-06
DLX3 [NCBI] 5.64053e-06
ID1 [NCBI] 5.63162e-06
TNFRSF11A [NCBI] 4.38634e-06
TNFSF11 [NCBI] 4.26003e-06
CTSL1 [NCBI] 4.18672e-06
AFP [NCBI] 3.81587e-06
PTH [NCBI] 2.80683e-06



OMIM


 OMIM Link Information
gain		 01
earlobes, thickened, with conductive deafness from incudostapedial abnormalities [NCBI] 0.00302164
HFM [NCBI] 0.00152628
BOS1 [NCBI] 0.000303961
SYM1 [NCBI] 0.000294489
BOR1 [NCBI] 0.000253147
ossicular malformations, familial [NCBI] 0.000227646
deafness, conductive stapedial, with ear malformation and facial palsy [NCBI] 0.000227646
stapes ankylosis with broad thumb and toes [NCBI] 0.000163944
wildervanck syndrome [NCBI] 0.000138768
hand-foot-uterus syndrome [NCBI] 0.000132793
deafness, conductive, with stapes fixation [NCBI] 0.000112578
TBS [NCBI] 0.000100967
AMC [NCBI] 9.48035e-05
DLX6 [NCBI] 6.89353e-05
DLX5 [NCBI] 5.94505e-05
EYA1 [NCBI] 5.07071e-05
AFP [NCBI] 1.98997e-05
PTH [NCBI] 1.2786e-05
RA [NCBI] 2.59728e-06
CF [NCBI] 4.21864e-07



Database Center for Life Science