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01 Ankylosis [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science