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MeSH keywords -> Related genes, diseases (OMIM)


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01 Glycogen Storage Disease [NCBI]

Gene


 Gene Link Information
Gain		 01
PHKG1P3 [NCBI] 0.000499621
PHKA1P1 [NCBI] 0.000499621
PHKG1P2 [NCBI] 0.000499621
PHKG1P1 [NCBI] 0.000499621
PHKA2 [NCBI] 0.000150703
SLC2A2 [NCBI] 0.000105224
PHKG2 [NCBI] 9.98431e-05
PRKAG2 [NCBI] 8.86178e-05
PHKB [NCBI] 6.21327e-05
AGL [NCBI] 3.65155e-05
PHKA1 [NCBI] 2.98708e-05
PHKG1 [NCBI] 2.49641e-05
PYGL [NCBI] 2.45578e-05
PYGM [NCBI] 2.00917e-05
SLC37A4 [NCBI] 1.73689e-05
GYS2 [NCBI] 1.32802e-05
PGAM2 [NCBI] 1.32802e-05
GYG2 [NCBI] 1.26968e-05
DNASE1L1 [NCBI] 1.26968e-05
PFKL [NCBI] 1.08058e-05
GYS1 [NCBI] 1.06496e-05
GBE1 [NCBI] 1.01372e-05
PFKM [NCBI] 1.003e-05
NHLRC1 [NCBI] 9.28329e-06
PRKAA1 [NCBI] 9.21733e-06
POLR2A [NCBI] 8.97635e-06
G6PC [NCBI] 8.66861e-06
LAMP2 [NCBI] 8.14686e-06
CS [NCBI] 6.62695e-06
FAH [NCBI] 6.29432e-06
SLC2A4 [NCBI] 5.00638e-06
BRCA1 [NCBI] 3.19085e-06



OMIM


 OMIM Link Information
gain		 01
glycogen storage disease ii [NCBI] 0.00299511
myopathy, autophagic vacuolar, infantile-onset [NCBI] 0.00252968
glycogen storage disease v [NCBI] 0.00168554
glycogen storage disease iii [NCBI] 0.00148275
glycogen storage disease ixa [NCBI] 0.00146546
glycogen storage disease iv [NCBI] 0.00143777
FBS [NCBI] 0.00137805
glycogen storage disease vii [NCBI] 0.000888893
phosphorylase kinase deficiency of liver and muscle, autosomal recessive [NCBI] 0.000473518
SLC2A2 [NCBI] 0.000472609
PHKG2 [NCBI] 0.000449826
danon disease [NCBI] 0.000423427
GAA [NCBI] 0.000351294
glycogen storage disease 0, liver [NCBI] 0.000336224
LAMP2 [NCBI] 0.000305651
PHKB [NCBI] 0.000299365
glycogen storage disease of heart, lethal congenital [NCBI] 0.000273629
glycogen storage disease i [NCBI] 0.000257258
glycogen storage disease vi [NCBI] 0.000251861
cardiomyopathy, familial hypertrophic, with wolff-parkinson-white syndrome [NCBI] 0.000232682
PYGM [NCBI] 0.000197808
PRKAG2 [NCBI] 0.000167417
PFKM [NCBI] 0.000157299
glycogen storage disease ib [NCBI] 0.00015271
glycogen storage disease ic [NCBI] 0.000125705
GYS2 [NCBI] 0.000121877
phosphoglycerate mutase, muscle, deficiency of [NCBI] 0.000107824
PHKA1 [NCBI] 0.000107824
polysaccharide, storage of unusual [NCBI] 0.000103248
glycogen storage disease 0, muscle [NCBI] 8.08034e-05
syringomas, multiple [NCBI] 7.2349e-05
muscle glycogenosis, x-linked [NCBI] 5.95637e-05
kanzaki disease [NCBI] 5.6877e-05
PGAM1 [NCBI] 5.23073e-05
sea-blue histiocyte disease [NCBI] 4.92038e-05
CMD3B [NCBI] 4.64311e-05
NHLRC1 [NCBI] 4.61456e-05
GYS1 [NCBI] 4.61456e-05
wolff-parkinson-white syndrome [NCBI] 4.30256e-05
GALE [NCBI] 3.96704e-05
AGL [NCBI] 3.89104e-05
G6PT1 [NCBI] 3.63514e-05
central core disease of muscle [NCBI] 3.35107e-05
myoclonic epilepsy of lafora [NCBI] 3.14923e-05
CMD1A [NCBI] 2.70713e-05
methemoglobinemia due to deficiency of methemoglobin reductase [NCBI] 2.58045e-05
mucolipidosis ii [NCBI] 2.34546e-05
hurler syndrome [NCBI] 2.10462e-05
metachromatic leukodystrophy [NCBI] 1.90203e-05
LPI [NCBI] 1.88347e-05



Database Center for Life Science