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MeSH keywords -> Related genes, diseases (OMIM)


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01 Muscular Diseases [NCBI]


Gene


Gene Link Information
Gain
01
WDM [NCBI] 0.00116424
TRNK [NCBI] 0.000720717
RP21 [NCBI] 0.000315643
MPD2 [NCBI] 0.000315643
RMD1 [NCBI] 0.000315643
ARVD7 [NCBI] 0.000315643
LOC619511 [NCBI] 0.000315643
RNR2 [NCBI] 0.000183789
CAV3 [NCBI] 0.000174013
MSTN [NCBI] 0.000150701
DYSF [NCBI] 0.000150555
MEG3 [NCBI] 0.000146954
MYOT [NCBI] 0.000142376
NA [NCBI] 0.000129056
DES [NCBI] 0.000125296
PKC [NCBI] 0.00011198
LAMP2 [NCBI] 8.81752e-05
MYH7 [NCBI] 8.22097e-05
SEPN1 [NCBI] 6.68668e-05
ATP2A1 [NCBI] 6.57394e-05
MTM1 [NCBI] 6.33152e-05
ACHE [NCBI] 6.32158e-05
RYR1 [NCBI] 6.08039e-05
SLCO1B1 [NCBI] 5.49712e-05
AMPD1 [NCBI] 4.98887e-05
COL6A2 [NCBI] 4.62002e-05
TAZ [NCBI] 4.36609e-05
CRYAB [NCBI] 4.35058e-05
COL6A1 [NCBI] 4.29589e-05
CPT2 [NCBI] 4.20036e-05
FHL1 [NCBI] 3.92824e-05
LMNA [NCBI] 3.66778e-05
LDB3 [NCBI] 3.60307e-05
PNPLA2 [NCBI] 3.48476e-05
CYP3A4 [NCBI] 2.48122e-05
DAG1 [NCBI] 2.37184e-05
FBXO32 [NCBI] 2.14369e-05
TRIM63 [NCBI] 2.14369e-05
GNE [NCBI] 2.089e-05
MAMLD1 [NCBI] 1.96328e-05
SYNC [NCBI] 1.96328e-05
MYOM2 [NCBI] 1.94346e-05
ITGA7 [NCBI] 1.90004e-05
MYH2 [NCBI] 1.90004e-05
CYP3A43 [NCBI] 1.90004e-05
SYNM [NCBI] 1.84675e-05
TYMP [NCBI] 1.84636e-05
COL6A3 [NCBI] 1.69116e-05
FLNC [NCBI] 1.63382e-05
CDH15 [NCBI] 1.56264e-05
MEFV [NCBI] 1.54661e-05
MB [NCBI] 1.48083e-05
TCAP [NCBI] 1.42394e-05
CYP3A5 [NCBI] 1.41239e-05
TTN [NCBI] 1.3713e-05
BIN1 [NCBI] 1.3713e-05
PYGM [NCBI] 1.31527e-05
ENO3 [NCBI] 1.30917e-05
GPRASP1 [NCBI] 1.30917e-05
DYSFIP1 [NCBI] 1.30917e-05
TRIM55 [NCBI] 1.30917e-05
CACNA1S [NCBI] 1.28563e-05
ACTA1 [NCBI] 1.28563e-05
CTSL1 [NCBI] 1.27349e-05
UBB [NCBI] 1.25839e-05
NOTCH3 [NCBI] 1.24595e-05
VCP [NCBI] 1.14165e-05
PAX7 [NCBI] 1.12954e-05
NOS1 [NCBI] 1.07857e-05
HSPB1 [NCBI] 1.07689e-05
MYOG [NCBI] 1.07486e-05
MYF6 [NCBI] 1.0712e-05
GLRX5 [NCBI] 1.0712e-05
RYR3 [NCBI] 1.0712e-05
SQSTM1 [NCBI] 1.03233e-05
PHKA1 [NCBI] 9.81432e-06
ATP5F1 [NCBI] 9.81432e-06
PIPOX [NCBI] 9.81432e-06
PGAM2 [NCBI] 9.81432e-06
SCN4A [NCBI] 9.60827e-06
SLC22A5 [NCBI] 9.30177e-06
MS [NCBI] 9.24645e-06
AMPD3 [NCBI] 9.23167e-06
ISCU [NCBI] 9.23167e-06
MYOZ3 [NCBI] 9.23167e-06
COX3 [NCBI] 9.23167e-06
MTMR3 [NCBI] 9.23167e-06
SLC44A1 [NCBI] 8.79863e-06
MYH3 [NCBI] 8.79863e-06
PTPLA [NCBI] 8.79863e-06
PHKB [NCBI] 8.79863e-06
DPP3 [NCBI] 8.79863e-06
IL28RA [NCBI] 8.79863e-06
COQ2 [NCBI] 8.79863e-06
MYOZ1 [NCBI] 8.79863e-06
ETFDH [NCBI] 8.79863e-06
IGF1 [NCBI] 8.62943e-06
MYOD1 [NCBI] 8.49931e-06
LETM1 [NCBI] 8.45371e-06
CRYM [NCBI] 8.45371e-06
LHX2 [NCBI] 8.45371e-06
IGF2AS [NCBI] 8.45371e-06
DNAJB6 [NCBI] 8.45371e-06
PRKAG3 [NCBI] 8.16701e-06
NAB1 [NCBI] 8.16701e-06
MAP4 [NCBI] 7.9217e-06
SOX6 [NCBI] 7.9217e-06
MYO1A [NCBI] 7.9217e-06
PGAM1 [NCBI] 7.9217e-06
TNNT1 [NCBI] 7.70733e-06
PRKAG1 [NCBI] 7.70733e-06
SLN [NCBI] 7.70733e-06
PHKG1 [NCBI] 7.70733e-06
COL15A1 [NCBI] 7.51697e-06
NDUFS4 [NCBI] 7.51697e-06
GARS [NCBI] 7.51697e-06
MYL3 [NCBI] 7.51697e-06
ATP2A3 [NCBI] 7.34581e-06
MAML1 [NCBI] 7.34581e-06
ABCB7 [NCBI] 7.34581e-06
MTMR1 [NCBI] 7.34581e-06
MAT1A [NCBI] 7.19032e-06
ACADS [NCBI] 7.19032e-06
SIL1 [NCBI] 7.0479e-06
PDF [NCBI] 7.0479e-06
ABP1 [NCBI] 6.91651e-06
SPTAN1 [NCBI] 6.91651e-06
NEB [NCBI] 6.79459e-06
MLF1 [NCBI] 6.79459e-06
MYL2 [NCBI] 6.79459e-06
POMGNT1 [NCBI] 6.79459e-06
PRKCH [NCBI] 6.79459e-06
EXOSC10 [NCBI] 6.79459e-06
GBE1 [NCBI] 6.68087e-06
TK2 [NCBI] 6.68087e-06
TRIM32 [NCBI] 6.68087e-06
REST [NCBI] 6.57431e-06
LAMB2 [NCBI] 6.47408e-06
ACADVL [NCBI] 6.47408e-06
SCN5A [NCBI] 6.45773e-06
COX2 [NCBI] 6.37947e-06
ANTXR2 [NCBI] 6.37947e-06
SERPINA6 [NCBI] 6.37947e-06
IGF2 [NCBI] 6.32815e-06
ABHD5 [NCBI] 6.20484e-06
KIF21A [NCBI] 6.20484e-06
LAMA2 [NCBI] 6.12387e-06
CSNK2B [NCBI] 6.12387e-06
MEF2C [NCBI] 6.04663e-06
CD276 [NCBI] 6.04663e-06
CACNA1C [NCBI] 5.97279e-06
COL9A3 [NCBI] 5.97279e-06
CAPN2 [NCBI] 5.97279e-06
MTMR2 [NCBI] 5.83419e-06
SCO2 [NCBI] 5.83419e-06
PPP1R3A [NCBI] 5.70619e-06
IGHMBP2 [NCBI] 5.70619e-06
LAMB1 [NCBI] 5.70619e-06
CLU [NCBI] 5.66017e-06
XK [NCBI] 5.64569e-06
GATM [NCBI] 5.5873e-06
CAPN1 [NCBI] 5.53089e-06
POLR2A [NCBI] 5.53089e-06
DMPK [NCBI] 5.48319e-06
NFATC1 [NCBI] 5.37229e-06
NBR1 [NCBI] 5.37229e-06
ANXA5 [NCBI] 5.37229e-06
DPP7 [NCBI] 5.27438e-06
SLC6A6 [NCBI] 5.22752e-06
PRKCZ [NCBI] 4.93209e-06
PLN [NCBI] 4.70334e-06
FKRP [NCBI] 4.55418e-06
HYOU1 [NCBI] 4.55418e-06
CSNK2A1 [NCBI] 4.5238e-06
AOC3 [NCBI] 4.35255e-06
XDH [NCBI] 4.27327e-06
LAMA1 [NCBI] 4.10222e-06
HSPD1 [NCBI] 4.10222e-06
IL15 [NCBI] 4.0792e-06
PLEC1 [NCBI] 4.01209e-06
TNNT2 [NCBI] 3.9268e-06
GH1 [NCBI] 3.88581e-06
MYH9 [NCBI] 3.76885e-06
TNFRSF4 [NCBI] 3.71348e-06
CAPN3 [NCBI] 3.66e-06
ATP2A2 [NCBI] 3.66e-06
LAMC2 [NCBI] 3.57473e-06
PHEX [NCBI] 3.47822e-06
LIF [NCBI] 3.35365e-06
CS [NCBI] 3.247e-06
CD24 [NCBI] 3.22041e-06
EIF4EBP1 [NCBI] 3.20729e-06
TRPV1 [NCBI] 3.18138e-06
PPARGC1A [NCBI] 3.03463e-06
ALOX5AP [NCBI] 3.03463e-06
DCK [NCBI] 3.03463e-06
TLR3 [NCBI] 2.85902e-06
CETP [NCBI] 2.78684e-06
DMD [NCBI] 2.60342e-06
CDKN1C [NCBI] 2.59477e-06
CYP2D6 [NCBI] 2.51921e-06
KLRK1 [NCBI] 2.51106e-06
CD22 [NCBI] 2.45528e-06
BID [NCBI] 2.34276e-06
FOXO1 [NCBI] 2.14837e-06
FABP7 [NCBI] 2.12977e-06
CACNA1A [NCBI] 2.12977e-06
FXN [NCBI] 2.01206e-06
IGFBP3 [NCBI] 1.97324e-06
LBP [NCBI] 1.91451e-06
FASLG [NCBI] 1.89832e-06
CYP2C9 [NCBI] 1.85338e-06
KCNQ1 [NCBI] 1.84842e-06
CAT [NCBI] 1.78313e-06
PRKCA [NCBI] 1.63101e-06
LPL [NCBI] 1.59963e-06
CDKN1B [NCBI] 1.42973e-06
BCL2 [NCBI] 1.42625e-06
GZMB [NCBI] 1.38537e-06
PMP22 [NCBI] 1.35893e-06
F8 [NCBI] 1.34918e-06
TNF [NCBI] 1.12703e-06
IL8 [NCBI] 1.06994e-06
HGF [NCBI] 1.06792e-06
BMP2 [NCBI] 9.8081e-07
APOB [NCBI] 7.96133e-07
PTGS1 [NCBI] 6.28697e-07
HLA-DQB1 [NCBI] 6.18712e-07
IL1B [NCBI] 6.07478e-07
BAX [NCBI] 6.01144e-07
FMR1 [NCBI] 5.4891e-07
VWF [NCBI] 5.47687e-07
PTGS2 [NCBI] 4.86973e-07
PTH [NCBI] 4.83274e-07
NGF [NCBI] 4.70598e-07
MPO [NCBI] 4.4821e-07
BRCA1 [NCBI] 4.07356e-07
CASP9 [NCBI] 3.76695e-07
CDKN1A [NCBI] 2.87793e-07
HLA-DRB1 [NCBI] 2.71582e-07
SOD1 [NCBI] 2.58109e-07
HRAS [NCBI] 2.38494e-07
CFTR [NCBI] 1.7194e-07
IL6 [NCBI] 1.52962e-07
CASP3 [NCBI] 1.16209e-07
NOS3 [NCBI] 1.08743e-07
APOE [NCBI] 9.86483e-08
PRL [NCBI] 6.20621e-08
NOS2 [NCBI] 5.00666e-08
HIF1A [NCBI] 4.14098e-08
EPO [NCBI] 1.26473e-08




OMIM


OMIM Link Information
gain
01
WDM [NCBI] 0.00452947
MEAX [NCBI] 0.0041494
myopathy, tubular aggregate [NCBI] 0.00389461
myopathy with deficiency of succinate dehydrogenase and aconitase [NCBI] 0.00317128
carnitine deficiency, myopathic [NCBI] 0.00285999
RMD1 [NCBI] 0.00228977
MTM1 [NCBI] 0.00196015
RMD [NCBI] 0.00179992
myopathy, myofibrillar, desmin-related [NCBI] 0.00172948
NEM3 [NCBI] 0.00172927
megaduodenum and/or megacystis [NCBI] 0.00161461
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases [NCBI] 0.001543
myopathy, distal, with onset in infancy [NCBI] 0.00152433
myopathy, hyaline body, autosomal recessive [NCBI] 0.00122532
MPD2 [NCBI] 0.00109085
myopathy, autophagic vacuolar, infantile-onset [NCBI] 0.00109085
marden-walker syndrome [NCBI] 0.00103274
RA [NCBI] 0.00100233
CFEOM3 [NCBI] 0.000824355
RSMD1 [NCBI] 0.00078249
cardiomyopathy associated with myopathy and sudden death [NCBI] 0.00076108
myopathy, congenital [NCBI] 0.00076108
central core disease of muscle [NCBI] 0.000757307
bethlem myopathy [NCBI] 0.00059511
CF [NCBI] 0.000572021
LGMD2L [NCBI] 0.000544359
singleton-merten syndrome [NCBI] 0.000544359
pallidopyramidal syndrome [NCBI] 0.000544359
DES [NCBI] 0.00053963
COL6A1 [NCBI] 0.00053855
BTHS [NCBI] 0.000514838
cayler cardiofacial syndrome [NCBI] 0.000495065
myopathy, myosin storage [NCBI] 0.000481686
minicore myopathy with external ophthalmoplegia [NCBI] 0.000481686
adducted thumbs syndrome [NCBI] 0.00046333
CAV3 [NCBI] 0.000453367
glycogen storage disease ii [NCBI] 0.000426128
mitochondrial myopathy [NCBI] 0.00042468
myopathy, centronuclear, autosomal dominant [NCBI] 0.00042468
MEHMO [NCBI] 0.000411145
SLE [NCBI] 0.000399834
MHS1 [NCBI] 0.000393386
GSM1 [NCBI] 0.000372658
KSS [NCBI] 0.000371454
visceral myopathy, familial, with external ophthalmoplegia [NCBI] 0.000342239
HMERF [NCBI] 0.000331488
alpha-b crystallinopathy [NCBI] 0.000331488
HMN7A [NCBI] 0.000317152
inclusion body myositis [NCBI] 0.000317152
RYR1 [NCBI] 0.000314284
glycogen storage disease vii [NCBI] 0.000302802
cataract and cardiomyopathy [NCBI] 0.000295853
MTM1 [NCBI] 0.000293417
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 0.000280383
AMPD1 [NCBI] 0.000277695
muscle glycogenosis, x-linked [NCBI] 0.000269773
native american myopathy [NCBI] 0.000269773
MELAS [NCBI] 0.000267609
CRYAB [NCBI] 0.000258106
myopathy, centronuclear, autosomal recessive [NCBI] 0.000254288
MTTL1 [NCBI] 0.000252276
myopathy with giant abnormal mitochondria [NCBI] 0.000248571
tibial muscular dystrophy, tardive [NCBI] 0.000243299
CDSP [NCBI] 0.000243294
MYH7 [NCBI] 0.000243199
mitochondrial myopathy with diabetes [NCBI] 0.000241987
COL6A2 [NCBI] 0.000237952
glycogen storage disease v [NCBI] 0.000237389
danon disease [NCBI] 0.00023358
brody myopathy [NCBI] 0.000222974
skin creases, multiple benign ring-shaped, of limbs [NCBI] 0.000221664
TAZ [NCBI] 0.000213348
megacystis-microcolon-intestinal hypoperistalsis syndrome [NCBI] 0.000210798
ATP2A1 [NCBI] 0.000207532
EKD1 [NCBI] 0.000193669
COL6A3 [NCBI] 0.000193624
ACHE [NCBI] 0.000187809
mitochondrial complex iii deficiency [NCBI] 0.000181446
MM [NCBI] 0.000175634
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 [NCBI] 0.000174437
CACNA1S [NCBI] 0.00016871
pleoconial myopathy with salt craving [NCBI] 0.000165684
minicore myopathy, antenatal onset, with arthrogryposis [NCBI] 0.000165684
MNGIE [NCBI] 0.00016415
HYPP [NCBI] 0.000163866
IBM3 [NCBI] 0.000163265
growth-mental deficiency syndrome of myhre [NCBI] 0.00015023
LGMD2H [NCBI] 0.00015023
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 0.00015023
TRIM32 [NCBI] 0.000143735
PHKA1 [NCBI] 0.000143735
glycogen storage disease iv [NCBI] 0.00014306
cerebrotendinous xanthomatosis [NCBI] 0.000140878
MSS [NCBI] 0.000138774
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 0.000135707
myopathy, spheroid body [NCBI] 0.000134827
myopathy with storage of glycoproteins and glycosaminoglycans [NCBI] 0.000134827
MTTK [NCBI] 0.000134315
mitochondrial complex iv deficiency [NCBI] 0.000131038
CFTD [NCBI] 0.000121519
coffin-siris syndrome [NCBI] 0.000120868
FMF [NCBI] 0.000112366
IBM2 [NCBI] 0.000110717
udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase [NCBI] 0.00010907
TTN [NCBI] 0.000107426
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 0.000106156
XK [NCBI] 0.000104391
LGMD1C [NCBI] 9.82852e-05
RCM1 [NCBI] 9.33449e-05
MPD1 [NCBI] 9.33449e-05
poland syndrome [NCBI] 9.27095e-05
TK2 [NCBI] 8.95192e-05
ETFDH [NCBI] 8.95192e-05
SEPN1 [NCBI] 8.58694e-05
phosphoglycerate mutase, muscle, deficiency of [NCBI] 8.58694e-05
glycogen storage disease iii [NCBI] 8.57382e-05
trismus-pseudocamptodactyly syndrome [NCBI] 8.53489e-05
myopathy, congenital, with crystalline intranuclear inclusions [NCBI] 8.28268e-05
neurologic disease, infantile multisystem, with osseous fragility [NCBI] 8.28268e-05
camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia [NCBI] 8.28268e-05
ataxia with fasciculations [NCBI] 8.28268e-05
hypermetabolism due to defect in mitochondria [NCBI] 8.28268e-05
myopathy due to malate-aspartate shuttle defect [NCBI] 8.28268e-05
dystonia with ringbinden [NCBI] 8.28268e-05
NLSDM [NCBI] 8.28268e-05
XMPMA [NCBI] 8.28268e-05
muscular dystrophy, cardiac type [NCBI] 8.28268e-05
muscular hypoplasia, congenital universal, of krabbe [NCBI] 8.28268e-05
amyotrophic dystonic paraplegia [NCBI] 8.28268e-05
myotilinopathy [NCBI] 8.28268e-05
stormorken syndrome [NCBI] 8.28268e-05
fingerprint body myopathy [NCBI] 8.28268e-05
gamstorp-wohlfart syndrome [NCBI] 8.28268e-05
mitochondrial myopathy with a defect in mitochondrial-protein transport [NCBI] 8.28268e-05
encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts [NCBI] 8.28268e-05
myopathy with abnormal lipid metabolism [NCBI] 8.28268e-05
TTID [NCBI] 8.27962e-05
TNF [NCBI] 8.07134e-05
parkinson disease, mitochondrial [NCBI] 7.90166e-05
MERRF [NCBI] 7.62864e-05
pena-shokeir syndrome, type i [NCBI] 7.42657e-05
mitochondrial dna depletion syndrome, myopathic form [NCBI] 7.37836e-05
phosphoglycerate kinase 1 deficiency [NCBI] 7.37836e-05
NM [NCBI] 7.37836e-05
DWS [NCBI] 7.15787e-05
CDS [NCBI] 7.14745e-05
CFEOM1 [NCBI] 7.14745e-05
thrombocytopenic purpura, autoimmune [NCBI] 7.14159e-05
coenzyme q10 deficiency [NCBI] 6.9332e-05
EDMD [NCBI] 6.74317e-05
pearson marrow-pancreas syndrome [NCBI] 6.73347e-05
APC [NCBI] 6.70397e-05
AHDS [NCBI] 6.54647e-05
mulibrey nanism [NCBI] 6.54647e-05
ENO3 [NCBI] 6.36884e-05
MYF6 [NCBI] 6.36884e-05
MYOG [NCBI] 6.36884e-05
AMPD3 [NCBI] 6.36884e-05
MTCYB [NCBI] 6.3081e-05
MSTN [NCBI] 6.20766e-05
BRRS [NCBI] 6.10608e-05
myotonia congenita, autosomal dominant [NCBI] 6.04843e-05
CMH10 [NCBI] 6.04523e-05
mental retardation, x-linked, with short stature, small testes, muscle wasting, and tremor [NCBI] 6.04523e-05
mitochondrial myopathy with lactic acidosis [NCBI] 6.04523e-05
erythrocyte lactate transporter defect [NCBI] 6.04523e-05
CMH8 [NCBI] 6.04523e-05
CDG2D [NCBI] 6.04523e-05
spinal muscular atrophy, scapuloperoneal [NCBI] 6.04523e-05
filaminopathy, autosomal dominant [NCBI] 6.04523e-05
anal sphincter myopathy, internal [NCBI] 6.04523e-05
LMNA [NCBI] 6.02957e-05
PMC [NCBI] 5.75877e-05
UCMD [NCBI] 5.62436e-05
DYSF [NCBI] 5.4174e-05
MADA [NCBI] 5.37346e-05
MB [NCBI] 5.31686e-05
HOKPP [NCBI] 5.25603e-05
myotubular myopathy with abnormal genital development [NCBI] 5.20682e-05
crisponi syndrome [NCBI] 5.20682e-05
alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus [NCBI] 5.20682e-05
neuropathy, ataxia, and retinitis pigmentosa [NCBI] 5.20682e-05
myopathy, congenital nonprogressive, with moebius sequence and robin sequence [NCBI] 5.20682e-05
LIMM [NCBI] 5.20682e-05
EXOSC10 [NCBI] 4.99241e-05
MYH2 [NCBI] 4.99241e-05
MTMR3 [NCBI] 4.99241e-05
NBR1 [NCBI] 4.99241e-05
MYL3 [NCBI] 4.99241e-05
POLG [NCBI] 4.96034e-05
VCP [NCBI] 4.91031e-05
CHNG2 [NCBI] 4.83106e-05
MADD [NCBI] 4.73451e-05
retinitis pigmentosa-deafness syndrome [NCBI] 4.6658e-05
corticosteroid-binding globulin deficiency [NCBI] 4.6658e-05
satoyoshi syndrome [NCBI] 4.6658e-05
HRAS [NCBI] 4.55234e-05
COL15A1 [NCBI] 4.4739e-05
FHL1 [NCBI] 4.4739e-05
FLNC [NCBI] 4.4739e-05
KY [NCBI] 4.4739e-05
LMO7 [NCBI] 4.4739e-05
UCHL3 [NCBI] 4.4739e-05
MTTV [NCBI] 4.4739e-05
SOX6 [NCBI] 4.4739e-05
MLASA [NCBI] 4.26602e-05
EDM3 [NCBI] 4.26602e-05
PGAM1 [NCBI] 4.13775e-05
ITGA7 [NCBI] 4.13775e-05
PHKB [NCBI] 4.13775e-05
CXORF6 [NCBI] 4.13775e-05
ETFB [NCBI] 4.13775e-05
CUL4B [NCBI] 4.13775e-05
PD [NCBI] 4.08186e-05
fumarase deficiency [NCBI] 3.94942e-05
phosphorylase kinase deficiency of liver and muscle, autosomal recessive [NCBI] 3.94942e-05
MAP4 [NCBI] 3.88822e-05
BIN1 [NCBI] 3.88822e-05
MYL2 [NCBI] 3.88822e-05
MTMR1 [NCBI] 3.88822e-05
COL9A3 [NCBI] 3.6897e-05
MTND2 [NCBI] 3.6897e-05
XBP1 [NCBI] 3.6897e-05
MTTH [NCBI] 3.6897e-05
EAD [NCBI] 3.68779e-05
SPMM [NCBI] 3.68779e-05
optic atrophy 1 and deafness [NCBI] 3.68779e-05
mitochondrial complex ii deficiency [NCBI] 3.68779e-05
SJS1 [NCBI] 3.66312e-05
PTH [NCBI] 3.56369e-05
SIL1 [NCBI] 3.52488e-05
SLN [NCBI] 3.52488e-05
ACTG1 [NCBI] 3.52488e-05
CRLF1 [NCBI] 3.52488e-05
aging [NCBI] 3.46523e-05
carnitine palmitoyltransferase i deficiency [NCBI] 3.46523e-05
CMRD [NCBI] 3.46523e-05
lactic acidosis, fatal infantile [NCBI] 3.46523e-05
IBMPFD [NCBI] 3.46523e-05
LSFC [NCBI] 3.46523e-05
MEG3 [NCBI] 3.38402e-05
SDHC [NCBI] 3.38402e-05
UBB [NCBI] 3.38402e-05
ACADM [NCBI] 3.37222e-05
DM2 [NCBI] 3.26289e-05
CACNA1C [NCBI] 3.26108e-05
costello syndrome [NCBI] 3.21092e-05
ACTA1 [NCBI] 3.15203e-05
GBE1 [NCBI] 3.15203e-05
LAMP2 [NCBI] 3.15203e-05
GARS [NCBI] 3.0541e-05
PNPLA2 [NCBI] 3.0541e-05
MTMR2 [NCBI] 3.0541e-05
PFKM [NCBI] 2.96524e-05
LDHA [NCBI] 2.96524e-05
SPG17 [NCBI] 2.94863e-05
hyperlysinemia [NCBI] 2.94863e-05
CPT2 [NCBI] 2.88394e-05
NEB [NCBI] 2.88394e-05
OPMD [NCBI] 2.85382e-05
schwannomatosis [NCBI] 2.81087e-05
trifunctional protein deficiency [NCBI] 2.81087e-05
lipomatosis, familial benign cervical [NCBI] 2.81087e-05
MTCO2 [NCBI] 2.80904e-05
LAMA2 [NCBI] 2.80904e-05
ACADVL [NCBI] 2.80904e-05
RP [NCBI] 2.78495e-05
HADHA [NCBI] 2.73961e-05
CD [NCBI] 2.71756e-05
congenital cataracts, facial dysmorphism, and neuropathy [NCBI] 2.68544e-05
methionine adenosyltransferase deficiency [NCBI] 2.68544e-05
SLC16A1 [NCBI] 2.55753e-05
NR4A3 [NCBI] 2.55753e-05
SLC22A5 [NCBI] 2.50391e-05
multiple pterygium syndrome, escobar variant [NCBI] 2.46435e-05
LGMD2B [NCBI] 2.46435e-05
PYGM [NCBI] 2.40512e-05
xanthinuria, type i [NCBI] 2.36602e-05
EA1 [NCBI] 2.36602e-05
OPA1 [NCBI] 2.35941e-05
SLC25A4 [NCBI] 2.35941e-05
acyl-coa dehydrogenase, very long-chain, deficiency of [NCBI] 2.27445e-05
ACADS [NCBI] 2.27425e-05
FTD [NCBI] 2.24026e-05
SCCMS [NCBI] 2.18885e-05
septooptic dysplasia [NCBI] 2.18885e-05
RYR2 [NCBI] 2.12453e-05
MTND1 [NCBI] 2.12453e-05
VED [NCBI] 2.10856e-05
oca2 gene [NCBI] 2.09066e-05
PLN [NCBI] 2.05801e-05
CAPN3 [NCBI] 2.05801e-05
DMD [NCBI] 1.99971e-05
fucosidosis [NCBI] 1.99608e-05
PRL [NCBI] 1.99491e-05
glycogen storage disease ixa [NCBI] 1.96665e-05
XPA [NCBI] 1.93816e-05
EDMD2 [NCBI] 1.89433e-05
lymphedema-distichiasis syndrome [NCBI] 1.89433e-05
MDC1A [NCBI] 1.83043e-05
GSD [NCBI] 1.83043e-05
NBIA1 [NCBI] 1.83043e-05
hyperekplexia, hereditary [NCBI] 1.83043e-05
SCN4A [NCBI] 1.7842e-05
MTATP6 [NCBI] 1.7842e-05
HNA [NCBI] 1.76974e-05
DMD [NCBI] 1.75292e-05
GAN1 [NCBI] 1.71199e-05
DMPK [NCBI] 1.63348e-05
BCL2 [NCBI] 1.57625e-05
hyperglycerolemia [NCBI] 1.55416e-05
mitochondrial complex i deficiency [NCBI] 1.55416e-05
SCN5A [NCBI] 1.54015e-05
APOA1 [NCBI] 1.54015e-05
CGL2 [NCBI] 1.50606e-05
PDB [NCBI] 1.50606e-05
MTND4 [NCBI] 1.48878e-05
EPO [NCBI] 1.42793e-05
HFTC [NCBI] 1.41574e-05
LGMD2C [NCBI] 1.3324e-05
PNKD1 [NCBI] 1.3324e-05
EFE [NCBI] 1.3324e-05
LBP [NCBI] 1.32405e-05
FPLD2 [NCBI] 1.29308e-05
DA2A [NCBI] 1.25521e-05
ZS [NCBI] 1.23538e-05
SMA3 [NCBI] 1.2187e-05
CHAC [NCBI] 1.18348e-05
MEB [NCBI] 1.14948e-05
OCA2 [NCBI] 1.11663e-05
COH1 [NCBI] 9.95651e-06
campomelic dysplasia [NCBI] 9.95651e-06
CMD1A [NCBI] 9.67765e-06
XPA [NCBI] 9.40735e-06
SERPINA6 [NCBI] 9.39539e-06
BMD [NCBI] 8.89098e-06
MAPT [NCBI] 8.70632e-06
CMH [NCBI] 7.77084e-06
CLN3 [NCBI] 7.72616e-06
DYT1 [NCBI] 7.51257e-06
CTNS [NCBI] 7.30486e-06
DCK [NCBI] 7.16194e-06
RSTS [NCBI] 5.83115e-06
PMP22 [NCBI] 5.57922e-06
NF2 [NCBI] 5.50872e-06
CLS [NCBI] 5.3536e-06
NGFB [NCBI] 5.20831e-06
MPO [NCBI] 4.91786e-06
PRNP [NCBI] 4.29988e-06
NPC1 [NCBI] 3.99893e-06
HGPS [NCBI] 3.88097e-06
FOP [NCBI] 3.65353e-06
WRN [NCBI] 3.54389e-06
PWS [NCBI] 2.77449e-06
CAT [NCBI] 2.58701e-06
LS [NCBI] 2.2584e-06
MUC1 [NCBI] 1.9837e-06
NF1 [NCBI] 1.56788e-06
G6PD [NCBI] 1.50892e-06
SMS [NCBI] 1.40351e-06
CDLS1 [NCBI] 8.76291e-07
FRAP1 [NCBI] 8.25605e-07
HGF [NCBI] 5.91694e-07
WBS [NCBI] 2.97005e-07
MG [NCBI] 1.30877e-07
SMAX1 [NCBI] 1.22305e-07
HD [NCBI] 3.27806e-08
APOB [NCBI] 2.25466e-08
TTR [NCBI] 7.89102e-09
LPL [NCBI] 1.06559e-09




Database Center for Life Science