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MeSH keywords -> Related genes, diseases (OMIM)


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01 Finger Joint [NCBI]

Gene


 Gene Link Information
Gain		 01
OA15 [NCBI] 0.000510938
OADIP [NCBI] 0.000510938
OA12 [NCBI] 0.000510938
OA18 [NCBI] 0.000510938
OA14 [NCBI] 0.000510938
OA19 [NCBI] 0.000510938
OA10 [NCBI] 0.000510938
OA13 [NCBI] 0.000510938
OA11 [NCBI] 0.000510938
OA20 [NCBI] 0.000510938
NOG [NCBI] 3.54083e-05
GDF5 [NCBI] 1.30356e-05
HFE [NCBI] 1.03728e-05
MPP6 [NCBI] 8.07864e-06
IL1RN [NCBI] 8.02642e-06
MATN3 [NCBI] 7.72659e-06
PRG4 [NCBI] 6.55511e-06
HLA-DQA1 [NCBI] 5.85581e-06
MSLN [NCBI] 5.41846e-06
HLA-C [NCBI] 5.32687e-06
ABCA1 [NCBI] 5.26806e-06
HLA-DQB1 [NCBI] 5.15992e-06
HLA-B [NCBI] 4.87896e-06
HLA-DRB1 [NCBI] 4.84104e-06
IL10 [NCBI] 4.08307e-06
CD68 [NCBI] 3.06764e-06



OMIM


 OMIM Link Information
gain		 01
RA [NCBI] 0.00277144
osteoarthropathy of fingers, familial [NCBI] 0.00256245
symphalangism, distal [NCBI] 0.0012021
spondyloepimetaphyseal dysplasia with multiple dislocations [NCBI] 0.00112601
CTS1 [NCBI] 0.000879846
SYM1 [NCBI] 0.000323031
CACP [NCBI] 0.000316516
HOA [NCBI] 0.000244083
SYNS1 [NCBI] 0.000204799
digital arthropathy-brachydactyly, familial [NCBI] 0.000175893
knuckle pads [NCBI] 0.000175893
dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism [NCBI] 0.000175893
symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch [NCBI] 0.000175893
syndesmodysplasic dwarfism [NCBI] 0.000175893
megaepiphyseal dwarfism [NCBI] 0.000175893
osteoarthritis of distal interphalangeal joints [NCBI] 0.000175893
arteritis, familial granulomatous, with juvenile polyarthritis [NCBI] 0.000175893
NOG [NCBI] 0.000164706
BDB2 [NCBI] 0.000136672
NPS [NCBI] 0.000123915
SLE [NCBI] 0.000120414
shprintzen-goldberg craniosynostosis syndrome [NCBI] 0.000112334
EPPK [NCBI] 8.15185e-05
osteoarthritis [NCBI] 7.66891e-05
pfeiffer syndrome [NCBI] 6.90472e-05
PPAC [NCBI] 6.90472e-05
TRPS1 [NCBI] 6.05987e-05
DA2A [NCBI] 5.61893e-05
IL1R1 [NCBI] 5.49754e-05
MATN3 [NCBI] 5.22392e-05
IL1A [NCBI] 4.82624e-05
PRG4 [NCBI] 4.33826e-05
fragile x mental retardation syndrome [NCBI] 2.35524e-05



Database Center for Life Science