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MeSH keywords -> Related genes, diseases (OMIM)


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01 Synostosis [NCBI]

Gene


 Gene Link Information
Gain		 01
MSSD [NCBI] 0.000499621
NOG [NCBI] 0.000119773
HOXD13 [NCBI] 6.12643e-05
FGFR2 [NCBI] 2.72451e-05
HOXA11 [NCBI] 2.50139e-05
POR [NCBI] 2.41279e-05
RASSF8 [NCBI] 1.40009e-05
FLNB [NCBI] 1.18101e-05
SSPN [NCBI] 1.08009e-05
GREM1 [NCBI] 1.00184e-05
GDF5 [NCBI] 9.31504e-06
FGFR1 [NCBI] 7.95279e-06
TWIST1 [NCBI] 7.47711e-06
FGFR3 [NCBI] 5.53945e-06
LIF [NCBI] 5.00998e-06



OMIM


 OMIM Link Information
gain		 01
cenani syndactylism [NCBI] 0.00396832
humeroradial synostosis [NCBI] 0.00214559
ABS [NCBI] 0.00124309
MSSD [NCBI] 0.00106493
mesomelia-synostoses syndrome [NCBI] 0.000847142
MF4 [NCBI] 0.000765046
mesomelic dysplasia, kantaputra type [NCBI] 0.000765046
symphalangism, distal [NCBI] 0.000765046
SYNS1 [NCBI] 0.000696285
radioulnar synostosis [NCBI] 0.000647607
spondylocarpotarsal synostosis syndrome [NCBI] 0.0005318
humeroradial synostosis [NCBI] 0.000358907
radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation [NCBI] 0.000358907
NOG [NCBI] 0.000350973
SYM1 [NCBI] 0.000241097
radioulnar synostosis with amegakaryocytic thrombocytopenia [NCBI] 0.000238978
TCC [NCBI] 0.000208033
SPD2 [NCBI] 0.000194053
por deficiency [NCBI] 0.00015794
FGFR2 [NCBI] 0.000133988
AFD1 [NCBI] 0.000129036
radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [NCBI] 0.000119344
SYNS2 [NCBI] 0.000119344
patella aplasia, coxa vara, and tarsal synostosis [NCBI] 0.000119344
radioulnar synostosis, unilateral, with developmental retardation and hypotonia [NCBI] 0.000119344
BDB2 [NCBI] 9.6882e-05
BDD [NCBI] 9.6882e-05
charge-like syndrome, x-linked [NCBI] 8.29119e-05
TS [NCBI] 8.29119e-05
humerospinal dysostosis [NCBI] 8.29119e-05
HOXA11 [NCBI] 7.77884e-05
BDE [NCBI] 7.05545e-05
muenke syndrome [NCBI] 6.67384e-05
lenz-majewski hyperostotic dwarfism [NCBI] 6.67384e-05
POR [NCBI] 5.92612e-05
DLL3 [NCBI] 5.65341e-05
HOXD13 [NCBI] 5.43977e-05
TWIST1 [NCBI] 4.94573e-05
GDF5 [NCBI] 4.90758e-05
SCDO1 [NCBI] 4.70281e-05
charge syndrome [NCBI] 4.47592e-05
SCS [NCBI] 4.20561e-05
FGFR1 [NCBI] 3.74876e-05
TD1 [NCBI] 3.32018e-05
ACP5 [NCBI] 2.278e-05
WBS [NCBI] 1.93896e-05



Database Center for Life Science