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MeSH keywords -> Related genes, diseases (OMIM)


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01 Foot Deformities [NCBI]

Gene


 Gene Link Information
Gain		 01
HOXA13 [NCBI] 3.92971e-05
FBXW4 [NCBI] 2.79295e-05
HOXD13 [NCBI] 2.30368e-05
LBX1 [NCBI] 1.88329e-05
KIAA1279 [NCBI] 1.55539e-05
HOXA3 [NCBI] 1.41909e-05
CUL4B [NCBI] 1.39034e-05
FBLN1 [NCBI] 1.06784e-05
GLI3 [NCBI] 9.49947e-06
COL1A2 [NCBI] 9.34437e-06
MPZ [NCBI] 8.97861e-06
SPAST [NCBI] 8.69004e-06
PMP22 [NCBI] 6.76168e-06
HTT [NCBI] 5.72807e-06
PTH [NCBI] 2.99718e-06



OMIM


 OMIM Link Information
gain		 01
SHFM3 [NCBI] 0.00154302
OFD3 [NCBI] 0.000938013
OFD5 [NCBI] 0.000938013
OFD9 [NCBI] 0.000813359
OFD4 [NCBI] 0.000711792
varadi-papp syndrome [NCBI] 0.000661222
HFM [NCBI] 0.000397016
FBXW4 [NCBI] 0.000167447
GCPS [NCBI] 0.000139887
uruguay faciocardiomusculoskeletal syndrome [NCBI] 0.00013578
cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss [NCBI] 0.00013578
GLI3 [NCBI] 0.000126586
ichthyosis, hystrix-like, with deafness [NCBI] 0.000113311
prader-willi habitus, osteopenia, and camptodactyly [NCBI] 0.000113311
OFD7 [NCBI] 0.000113311
mental retardation, x-linked, with short stature, small testes, muscle wasting, and tremor [NCBI] 0.000113311
ehlers-danlos syndrome, autosomal recessive, cardiac valvular form [NCBI] 0.000104833
acrorenal-mandibular syndrome [NCBI] 9.52359e-05
polydactyly, preaxial iv [NCBI] 9.52359e-05
goldberg-shprintzen megacolon syndrome [NCBI] 8.92647e-05
lenz-majewski hyperostotic dwarfism [NCBI] 8.31153e-05
CUL4B [NCBI] 7.45227e-05
BTRC [NCBI] 7.20115e-05
PDP [NCBI] 7.06814e-05
BGS [NCBI] 6.7806e-05
ACLS [NCBI] 6.7161e-05
HOXA13 [NCBI] 6.35753e-05
SPG4 [NCBI] 6.22932e-05
TBS [NCBI] 6.13869e-05
COL1A2 [NCBI] 4.36109e-05
FGFR2 [NCBI] 3.82888e-05
BCNS [NCBI] 3.68878e-05
RA [NCBI] 2.0374e-05
TS [NCBI] 1.98042e-05
PTH [NCBI] 7.00447e-06



Database Center for Life Science