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MeSH keywords -> Related genes, diseases (OMIM)


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01 Dysostoses [NCBI]

Gene


 Gene Link Information
Gain		 01
DLL3 [NCBI] 0.000130808
CTSK [NCBI] 3.72461e-05
MESP2 [NCBI] 3.65621e-05
HES7 [NCBI] 1.82381e-05
LFNG [NCBI] 1.58576e-05
CHST3 [NCBI] 1.49592e-05
STK32B [NCBI] 1.49592e-05
EVC [NCBI] 1.18154e-05
PAX1 [NCBI] 1.11009e-05
SBDS [NCBI] 1.00053e-05
PAX9 [NCBI] 9.75468e-06
HOXD13 [NCBI] 9.65757e-06
CTSA [NCBI] 9.45036e-06
TSC2 [NCBI] 8.01071e-06
PKD1 [NCBI] 6.02062e-06
EGF [NCBI] 2.31835e-06



OMIM


 OMIM Link Information
gain		 01
acrodysostosis [NCBI] 0.00320713
POADS [NCBI] 0.00201121
costovertebral segmentation anomalies [NCBI] 0.00162737
SCDO1 [NCBI] 0.00133155
dysosteosclerosis [NCBI] 0.000807657
DLL3 [NCBI] 0.000678207
OSCS [NCBI] 0.000601472
varadi-papp syndrome [NCBI] 0.000450881
short rib-polydactyly syndrome, type ii [NCBI] 0.000440615
pelvis-shoulder dysplasia [NCBI] 0.000314637
SCDO3 [NCBI] 0.000254219
SDS [NCBI] 0.000244853
CTSK [NCBI] 0.000198588
acrofacial dysostosis syndrome of rodriguez [NCBI] 0.000186362
pycnodysostosis [NCBI] 0.000152532
spondylospinal thoracic dysostosis [NCBI] 0.000126878
fibuloulnar aplasia or hypoplasia with renal abnormalities [NCBI] 0.000126878
SCDO2 [NCBI] 0.000126878
spinal dysplasia, anhalt type [NCBI] 0.000126878
pelviscapular dysplasia [NCBI] 0.000104412
spondylocostal dysostosis with anal atresia and urogenital anomalies [NCBI] 9.59359e-05
MESP2 [NCBI] 9.22788e-05
mesoderm posterior 1 [NCBI] 9.22788e-05
robin sequence with cleft mandible and limb anomalies [NCBI] 9.0434e-05
weyers acrofacial dysostosis [NCBI] 8.30867e-05
weyers ulnar ray/oligodactyly syndrome [NCBI] 8.30867e-05
LFNG [NCBI] 7.8499e-05
CRMP1 [NCBI] 7.8499e-05
frontonasal dysplasia [NCBI] 7.80613e-05
EVC [NCBI] 6.74106e-05
PFM [NCBI] 6.74103e-05
robinow syndrome, autosomal recessive [NCBI] 6.10678e-05
NOTCH3 [NCBI] 5.80724e-05
EVC [NCBI] 5.17308e-05
PHS [NCBI] 4.97833e-05
JAG1 [NCBI] 4.83906e-05
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 4.5103e-05
ALGS1 [NCBI] 4.23532e-05
CHH [NCBI] 4.19061e-05
apnea, obstructive sleep [NCBI] 2.27475e-05
EGF [NCBI] 3.0969e-06



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