Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Ankylosis	[NCBI]

Gene	Link	Information Gain
FOP	[NCBI]	0.000815663
NOG	[NCBI]	9.64026e-05
ANKH	[NCBI]	3.69525e-05
GDF5	[NCBI]	2.20514e-05
BMP3	[NCBI]	1.11152e-05
ENPP1	[NCBI]	7.89275e-06
TJP1	[NCBI]	7.00069e-06
BMP7	[NCBI]	6.93267e-06
CKAP4	[NCBI]	6.93267e-06
MATN1	[NCBI]	6.87312e-06
F8	[NCBI]	6.24491e-06
TP63	[NCBI]	6.20504e-06
TNFRSF11A	[NCBI]	5.48801e-06
TNFSF11	[NCBI]	5.25136e-06
TNFRSF11B	[NCBI]	5.20955e-06

OMIM	Link	Information gain
pena-shokeir syndrome, type i	[NCBI]	0.00436531
symphalangism, distal	[NCBI]	0.00171781
molar i reinclusion	[NCBI]	0.00148945
lethal congenital contracture syndrome 1	[NCBI]	0.000579915
OTSC1	[NCBI]	0.000479378
CGF	[NCBI]	0.000400829
SYM1	[NCBI]	0.000384947
stapes ankylosis with broad thumb and toes	[NCBI]	0.000353199
NOG	[NCBI]	0.000308074
FOP	[NCBI]	0.000183908
SYNS1	[NCBI]	0.000168802
SPDA1	[NCBI]	0.000132394
syndesmodysplasic dwarfism	[NCBI]	0.000129339
symphalangism, c. s. lewis type	[NCBI]	0.000129339
BDB2	[NCBI]	0.000106872
thumbs, stiff, with brachydactyly type a1 and developmental delay	[NCBI]	0.000106872
por deficiency	[NCBI]	7.66903e-05
BDA1	[NCBI]	7.66903e-05
CLPED1	[NCBI]	7.5072e-05
ankyloblepharon-ectodermal defects-cleft lip/palate	[NCBI]	7.5072e-05
adult syndrome	[NCBI]	7.22548e-05
LADD	[NCBI]	7.22548e-05
LMS	[NCBI]	6.98586e-05
COFS1	[NCBI]	6.87826e-05
EEC3	[NCBI]	6.77742e-05
ANKH	[NCBI]	6.724e-05
POR	[NCBI]	6.724e-05
CMDD	[NCBI]	6.42765e-05
deafness, conductive, with stapes fixation	[NCBI]	6.27781e-05
PPAC	[NCBI]	6.27781e-05
ABS	[NCBI]	5.84247e-05
CCAL2	[NCBI]	5.84247e-05
TP73L	[NCBI]	5.78247e-05
apnea, obstructive sleep	[NCBI]	5.72227e-05
FMF	[NCBI]	4.37193e-05
RA	[NCBI]	4.19609e-05
osteogenesis imperfecta, type i	[NCBI]	4.16654e-05
FGFR2	[NCBI]	4.09413e-05