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MeSH keywords -> Related genes, diseases (OMIM)


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01 Spasms, Infantile [NCBI]

Gene


 Gene Link Information
Gain		 01
BFIC [NCBI] 0.000345139
ARX [NCBI] 0.000279784
CDKL5 [NCBI] 0.000146987
TRH [NCBI] 2.76151e-05
PAFAH1B1 [NCBI] 2.57429e-05
CRH [NCBI] 2.35011e-05
SCN1A [NCBI] 1.67482e-05
CDKL2 [NCBI] 1.39161e-05
CDKL1 [NCBI] 1.30177e-05
CDKL3 [NCBI] 1.30177e-05
PHGDH [NCBI] 1.24344e-05
MECP2 [NCBI] 1.08193e-05
MAGI2 [NCBI] 1.07154e-05
SLC2A1 [NCBI] 1.06874e-05
MOCS1 [NCBI] 1.05435e-05
CLCA2 [NCBI] 1.02442e-05
PDCD6IP [NCBI] 9.9895e-06
MC2R [NCBI] 9.87506e-06
SLC6A1 [NCBI] 9.39548e-06
SCN2A [NCBI] 9.23586e-06
NHLRC1 [NCBI] 9.02129e-06
HSD17B4 [NCBI] 8.50333e-06
KCNQ3 [NCBI] 8.31546e-06
LGI1 [NCBI] 7.85109e-06
PTCH1 [NCBI] 7.35502e-06
TSC1 [NCBI] 7.30514e-06
NDP [NCBI] 7.28074e-06
ELN [NCBI] 7.14125e-06
ATP1A2 [NCBI] 7.09719e-06
SLC22A5 [NCBI] 6.62566e-06
MC4R [NCBI] 6.46857e-06
KCNJ11 [NCBI] 6.21811e-06
TSC2 [NCBI] 6.08158e-06
NF1 [NCBI] 6.08158e-06
TIMP1 [NCBI] 5.9664e-06
CYP2C19 [NCBI] 4.90085e-06
MMP9 [NCBI] 3.79852e-06
TH [NCBI] 2.4935e-06
AVP [NCBI] 2.42083e-06
GFAP [NCBI] 1.6521e-06
PRL [NCBI] 1.38965e-06
TNF [NCBI] 1.55555e-07



OMIM


 OMIM Link Information
gain		 01
AIC [NCBI] 0.00460935
peho syndrome [NCBI] 0.00431394
infantile spasm syndrome, x-linked [NCBI] 0.00142123
EKD1 [NCBI] 0.00105279
TS [NCBI] 0.000850952
MHAC [NCBI] 0.000676229
ICCA [NCBI] 0.000623113
EKD2 [NCBI] 0.000552346
microcephaly, hiatus hernia, and nephrotic syndrome [NCBI] 0.000484704
FEB1 [NCBI] 0.000425256
ARX [NCBI] 0.000365507
CDKL5 [NCBI] 0.000357192
myoclonic epilepsy, neonatal, with suppression-burst pattern [NCBI] 0.000342288
EBN1 [NCBI] 0.000218605
rett syndrome, atypical, cdkl5-related [NCBI] 0.000193479
CRH [NCBI] 0.000161135
FSHMD1A [NCBI] 0.000131291
mental and growth retardation with amblyopia [NCBI] 9.65978e-05
microcephaly, corpus callosum dysgenesis, and cleft lip/palate [NCBI] 8.8126e-05
CLN10 [NCBI] 8.26281e-05
simpson-golabi-behmel syndrome, type 2 [NCBI] 8.26281e-05
EBN2 [NCBI] 8.26281e-05
PHGDH [NCBI] 7.07276e-05
microcephaly with spastic quadriplegia [NCBI] 7.02714e-05
ACCPN [NCBI] 6.20348e-05
EPD [NCBI] 5.85774e-05
SPD1 [NCBI] 5.85774e-05
molybdenum cofactor deficiency [NCBI] 5.85774e-05
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis [NCBI] 5.7574e-05
MTTF [NCBI] 5.59803e-05
PRPS1 [NCBI] 5.45574e-05
HSD17B4 [NCBI] 5.33135e-05
hyperekplexia, hereditary [NCBI] 5.26074e-05
orotic aciduria i [NCBI] 4.67316e-05
SGBS1 [NCBI] 4.62686e-05
mitochondrial complex iv deficiency [NCBI] 4.53493e-05
SMEI [NCBI] 4.32651e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 3.88873e-05
FLNA [NCBI] 3.88776e-05
HHF2 [NCBI] 3.72265e-05
ND [NCBI] 3.52646e-05
ELN [NCBI] 3.40655e-05
LS [NCBI] 3.04168e-05
WT1 [NCBI] 2.96153e-05
SMS [NCBI] 2.84202e-05
MECP2 [NCBI] 2.65487e-05
AS [NCBI] 1.22905e-05
TH [NCBI] 5.99391e-06
panencephalitis, subacute sclerosing [NCBI] 5.02174e-06
AVP [NCBI] 3.83682e-06
GFAP [NCBI] 2.53489e-06
PRL [NCBI] 1.42491e-06
VEGF [NCBI] 1.30071e-06
TNF [NCBI] 7.00003e-07



Database Center for Life Science