Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ankle [NCBI]

Gene


 Gene Link Information
Gain		 01
AIS [NCBI] 0.000184137
MS [NCBI] 8.56388e-05
EDIL3 [NCBI] 8.26699e-06
KCNJ12 [NCBI] 7.65502e-06
HYAL1 [NCBI] 7.59937e-06
F13A1 [NCBI] 6.97542e-06
SS18 [NCBI] 6.53628e-06
DLG1 [NCBI] 5.50822e-06
CD99 [NCBI] 5.09297e-06
SERPINE1 [NCBI] 4.7494e-06
CNN1 [NCBI] 4.4612e-06
NOG [NCBI] 4.13532e-06
TNFRSF11B [NCBI] 3.9145e-06
CCL2 [NCBI] 3.82327e-06
PTGS1 [NCBI] 3.80503e-06
CD68 [NCBI] 3.25301e-06
NOS3 [NCBI] 3.16331e-06
TRH [NCBI] 2.96391e-06
PTGS2 [NCBI] 2.38109e-06



OMIM


 OMIM Link Information
gain		 01
osteolysis, hereditary, of carpal bones with nephropathy [NCBI] 0.0021953
arthrogryposis-like disorder [NCBI] 0.00163019
clubbing of digits [NCBI] 0.00131934
DA2A [NCBI] 0.000382835
IS1 [NCBI] 0.000351307
STALE [NCBI] 0.00021531
patella aplasia, coxa vara, and tarsal synostosis [NCBI] 0.00021531
hyaluronan metabolism, defect in [NCBI] 0.000176047
hyaluronidase deficiency [NCBI] 0.000176047
yellow nail syndrome [NCBI] 0.000161236
SPD2 [NCBI] 0.000151622
noonan-like/multiple giant cell lesion syndrome [NCBI] 0.000134056
SEDT [NCBI] 0.000123331
hand-foot-uterus syndrome [NCBI] 0.000120507
EDM1 [NCBI] 0.000117942
SYM1 [NCBI] 0.000113424
hypertrophic neuropathy of dejerine-sottas [NCBI] 8.33622e-05
HYAL1 [NCBI] 6.51671e-05
DFSP [NCBI] 5.61936e-05
NOG [NCBI] 5.08425e-05
FMF [NCBI] 4.04893e-05
FRAP1 [NCBI] 2.82408e-05
CD [NCBI] 2.55223e-05
PWS [NCBI] 2.13589e-05
SLE [NCBI] 1.70024e-05
RA [NCBI] 6.34376e-07



Database Center for Life Science