Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Ear Ossicles	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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