Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Carpal Bones	[NCBI]

Gene	Link	Information Gain
DURS1	[NCBI]	0.000510938
NOG	[NCBI]	1.59192e-05
SHOX	[NCBI]	1.37014e-05
MATN1	[NCBI]	1.0711e-05
CFC1	[NCBI]	7.49658e-06
ANKH	[NCBI]	7.06649e-06
MLPH	[NCBI]	6.94682e-06
HOXD13	[NCBI]	6.67663e-06
COMP	[NCBI]	5.15203e-06
FGFR3	[NCBI]	4.607e-06
IL1B	[NCBI]	4.40883e-06
TNF	[NCBI]	4.23596e-06
CD68	[NCBI]	3.25301e-06

OMIM	Link	Information gain
osteolysis, hereditary, of carpal bones with nephropathy	[NCBI]	0.00621054
hydrocephalus, autosomal dominant	[NCBI]	0.00148718
mesomelic dysplasia, kantaputra type	[NCBI]	0.00105937
spondylometaphyseal dysplasia, kozlowski type	[NCBI]	0.00105937
DURS1	[NCBI]	0.000738236
spondylocarpotarsal synostosis syndrome	[NCBI]	0.00067775
ATD1	[NCBI]	0.000504545
patent ductus arteriosus and bicuspid aortic valve with hand anomalies	[NCBI]	0.000202202
BDA6	[NCBI]	0.000202202
symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch	[NCBI]	0.000202202
bor-duane hydrocephalus contiguous gene syndrome	[NCBI]	0.000202202
megaepiphyseal dwarfism	[NCBI]	0.000202202
osteoid osteoma	[NCBI]	0.000202202
LWD	[NCBI]	0.000195634
devriendt syndrome	[NCBI]	0.000162947
second metatarsal-metacarpal syndrome	[NCBI]	0.000162947
humeroradial synostosis	[NCBI]	0.000162947
TCC	[NCBI]	0.000148144
MADB	[NCBI]	0.000138539
winchester syndrome	[NCBI]	0.000131402
RA	[NCBI]	0.00011957
spondyloepimetaphyseal dysplasia, strudwick type	[NCBI]	0.000110298
weaver syndrome	[NCBI]	0.000100424
chondrodysplasia punctata, autosomal dominant	[NCBI]	9.84211e-05
BGS	[NCBI]	8.37791e-05
EVC	[NCBI]	8.26677e-05
DA2A	[NCBI]	8.16e-05
BOR1	[NCBI]	8.05727e-05
CRMO	[NCBI]	7.05796e-05
HOS	[NCBI]	6.49643e-05
HHT	[NCBI]	6.38639e-05
HOXA11	[NCBI]	5.96594e-05
HOXD13	[NCBI]	4.64755e-05
NOG	[NCBI]	4.28919e-05
GJA5	[NCBI]	4.16036e-05
SLE	[NCBI]	3.94837e-05
FGFR3	[NCBI]	2.99965e-05
COMP	[NCBI]	2.79085e-05
TTR	[NCBI]	2.3648e-05
TNF	[NCBI]	3.1454e-06