Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Osteoarthropathy, Secondary Hypertrophic [NCBI]

Gene


 Gene Link Information
Gain		 01
CA9 [NCBI] 8.70047e-06
FGFR3 [NCBI] 7.62409e-06
SMAD4 [NCBI] 7.57917e-06
ACP5 [NCBI] 7.25143e-06
IL1RN [NCBI] 5.64074e-06
HIF1A [NCBI] 5.57385e-06
HGF [NCBI] 5.54804e-06
TGFB1 [NCBI] 5.17252e-06
VEGFA [NCBI] 4.87401e-06
PTGS2 [NCBI] 4.06936e-06



OMIM


 OMIM Link Information
gain		 01
broad terminal phalanges, familial [NCBI] 0.00129156
clubbing of digits [NCBI] 0.00107364
thrombocytopenia-absent radius syndrome [NCBI] 0.000598023
PDP [NCBI] 0.000167038
cyanosis and hepatic disease [NCBI] 0.000136591
osteoarthropathy, familial idiopathic, of childhood [NCBI] 0.000136591
VEGF [NCBI] 0.000102728
PTHS [NCBI] 9.6046e-05
JPHT [NCBI] 9.27854e-05
GHRH [NCBI] 7.71756e-05
LRS1 [NCBI] 7.60048e-05
CF [NCBI] 7.54435e-05
HSAN2 [NCBI] 7.40438e-05
pulmonary fibrosis, idiopathic [NCBI] 6.61745e-05
JPS [NCBI] 5.60514e-05
BGLAP [NCBI] 3.71254e-05
HGF [NCBI] 1.3016e-05
AVP [NCBI] 1.182e-05
SLE [NCBI] 9.43832e-06
RA [NCBI] 7.06708e-08



Database Center for Life Science