Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Wrist	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000228906
NEWENTRY	[NCBI]	0.000136981
SHOX	[NCBI]	1.50943e-05
GDAP1	[NCBI]	7.79269e-06
KRT1	[NCBI]	7.29492e-06
COL1A1	[NCBI]	6.04253e-06
PRNP	[NCBI]	5.67605e-06
ADIPOQ	[NCBI]	5.61265e-06
PPARG	[NCBI]	5.19521e-06
NOG	[NCBI]	4.79311e-06
ESR1	[NCBI]	4.60454e-06
VDR	[NCBI]	4.29301e-06

OMIM	Link	Information gain
osteolysis, hereditary, of carpal bones with nephropathy	[NCBI]	0.00201127
synostosis, carpal, with dysplastic elbow joints and brachydactyly	[NCBI]	0.00123667
bone size quantitative trait locus 1	[NCBI]	0.0011195
collagenosis, familial reactive perforating	[NCBI]	0.000987008
LWD	[NCBI]	0.000891838
DBQD	[NCBI]	0.000820071
RA	[NCBI]	0.000674251
DA2A	[NCBI]	0.000313703
genu valgum, st. helena familial	[NCBI]	0.000153522
S PEAK SYNDROME	[NCBI]	0.000153522
ankylosing vertebral hyperostosis with tylosis	[NCBI]	0.000138729
pneumothorax, primary spontaneous	[NCBI]	0.000122005
langer mesomelic dysplasia	[NCBI]	0.000116331
trismus-pseudocamptodactyly syndrome	[NCBI]	0.000111618
SHOX	[NCBI]	9.93179e-05
hand-foot-uterus syndrome	[NCBI]	9.81379e-05
EDM1	[NCBI]	9.55898e-05
SYM1	[NCBI]	9.11068e-05
hypophosphatemic rickets, x-linked dominant	[NCBI]	6.5975e-05
apnea, obstructive sleep	[NCBI]	6.32481e-05
HOS	[NCBI]	5.59589e-05
MYH8	[NCBI]	5.37697e-05
CDLS1	[NCBI]	4.79757e-05
NOG	[NCBI]	4.39233e-05
COL1A1	[NCBI]	3.79502e-05
CCL22	[NCBI]	3.49753e-05
VDR	[NCBI]	1.84588e-05
SLE	[NCBI]	1.40771e-05
PWS	[NCBI]	6.20203e-06
PD	[NCBI]	5.09823e-06
AD	[NCBI]	1.32432e-06