Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Histocytochemistry [NCBI]


Gene


Gene Link Information
Gain
01




OMIM


OMIM Link Information
gain
01
ACHE [NCBI] 0.0052221
corneal dystrophy, crystalline, of schnyder [NCBI] 0.00133596
red skin pigment anomaly of new guinea [NCBI] 0.0011398
myopathy, distal, with onset in infancy [NCBI] 0.0011398
CHAT [NCBI] 0.0010928
myopathy, hyaline body, autosomal recessive [NCBI] 0.000875062
spondylodysplasia with pure brachyolmia [NCBI] 0.000875062
neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers [NCBI] 0.00077544
gangliosidosis, gm2, type iii, or juvenile type [NCBI] 0.00077544
peeling skin syndrome [NCBI] 0.000710915
CEACAM5 [NCBI] 0.000667978
myopathy, tubular aggregate [NCBI] 0.000663058
HLP [NCBI] 0.000663058
CDAN3 [NCBI] 0.000625019
carnitine deficiency, myopathic [NCBI] 0.000566527
WDM [NCBI] 0.000503535
DYT2 [NCBI] 0.000486602
GFAP [NCBI] 0.000484621
IBGC1 [NCBI] 0.000471124
TH [NCBI] 0.000419016
IGAN1 [NCBI] 0.000409146
small cell cancer of the lung [NCBI] 0.000389406
glycogen storage disease ii [NCBI] 0.000383824
alport syndrome, autosomal dominant [NCBI] 0.00038032
ACP5 [NCBI] 0.000374252
hashimoto thyroiditis [NCBI] 0.000363476
glycogen storage disease iv [NCBI] 0.000331104
CHS [NCBI] 0.000308787
MUC1 [NCBI] 0.000303904
sea-blue histiocyte disease [NCBI] 0.00025839
TNF [NCBI] 0.000253185
KSS [NCBI] 0.000239401
VEGF [NCBI] 0.000229499
SLE [NCBI] 0.00022913
mucopolysaccharidosis type vi [NCBI] 0.000226908
G6PD [NCBI] 0.000210824
gm1-gangliosidosis, type ii [NCBI] 0.000203867
myeloperoxidase deficiency [NCBI] 0.000197207
mitochondrial complex iv deficiency [NCBI] 0.000192681
CLN3 [NCBI] 0.000185534
CF [NCBI] 0.000169694
ENPEP [NCBI] 0.000166929
CLN2 [NCBI] 0.00016102
cystinosis, adult nonnephropathic [NCBI] 0.000149874
central core disease of muscle [NCBI] 0.000143801
NPY [NCBI] 0.000140983
peroxidase and phospholipid deficiency in eosinophils [NCBI] 0.000140866
corneal dystrophy, epithelial basement membrane [NCBI] 0.000140866
wolman disease [NCBI] 0.000133896
EGFR [NCBI] 0.000127481
mitochondrial myopathy [NCBI] 0.000122135
mucolipidosis ii [NCBI] 0.000118466
CDL1 [NCBI] 0.000113334
myopathy, congenital, with crystalline intranuclear inclusions [NCBI] 0.000108481
dystonia with ringbinden [NCBI] 0.000108481
myopathy with storage of glycoproteins and glycosaminoglycans [NCBI] 0.000108481
glycoprotein storage disease [NCBI] 0.000108481
ovalocytosis, hereditary hemolytic [NCBI] 0.000108481
metachromasia of fibroblasts [NCBI] 0.000108481
myopathy with abnormal lipid metabolism [NCBI] 0.000108481
myotonic myopathy with cylindrical spirals [NCBI] 0.000108481
PNMT [NCBI] 0.000106
AFP [NCBI] 0.000105698
CDS [NCBI] 0.00010306
SGD [NCBI] 0.00010306
niemann-pick disease, type b [NCBI] 0.00010306
MTM1 [NCBI] 9.90964e-05
NPC1 [NCBI] 9.69833e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 8.93155e-05
PMC [NCBI] 8.83673e-05
GAL [NCBI] 8.6888e-05
gm1-gangliosidosis, type i [NCBI] 8.63992e-05
mucolipidosis iv [NCBI] 8.45316e-05
CLN1 [NCBI] 8.27552e-05
glycogen storage disease iii [NCBI] 8.27552e-05
glycogen storage disease v [NCBI] 8.10619e-05
glycogen storage disease ib [NCBI] 8.10619e-05
VIP [NCBI] 8.10481e-05
pleoconial myopathy with salt craving [NCBI] 8.07964e-05
myopathy with giant abnormal mitochondria [NCBI] 8.07964e-05
hypermetabolism due to defect in mitochondria [NCBI] 8.07964e-05
corneal dystrophy, juvenile epithelial, of meesmann [NCBI] 8.07964e-05
neuronal intranuclear inclusion disease [NCBI] 8.07964e-05
cardiomyopathy, infantile histiocytoid [NCBI] 8.07964e-05
ACPP [NCBI] 7.96852e-05
NEM3 [NCBI] 7.94445e-05
myoclonic epilepsy of lafora [NCBI] 7.49895e-05
RA [NCBI] 7.229e-05
LIMM [NCBI] 7.04025e-05
AR [NCBI] 7.01392e-05
fabry disease [NCBI] 6.98333e-05
glycogen storage disease vii [NCBI] 6.86241e-05
EGF [NCBI] 6.503e-05
OPMD [NCBI] 6.48108e-05
amyloidosis, familial visceral [NCBI] 6.3684e-05
thyroid hormonogenesis, genetic defect in, 5 [NCBI] 6.3684e-05
corpus callosum, partial agenesis of, x-linked [NCBI] 6.3684e-05
corneal fleck dystrophy [NCBI] 6.3684e-05
EPO [NCBI] 5.9927e-05
HGF [NCBI] 5.92193e-05
APBD [NCBI] 5.8711e-05
CSCD [NCBI] 5.8711e-05
schindler disease, type i [NCBI] 5.8711e-05
NN [NCBI] 5.8711e-05
mitochondrial complex ii deficiency [NCBI] 5.8711e-05
eunuchoidism, familial hypogonadotropic [NCBI] 5.8711e-05
thyrotropin deficiency, isolated [NCBI] 5.47662e-05
creatine phosphokinase, elevated serum [NCBI] 5.47662e-05
mitochondrial complex iii deficiency [NCBI] 5.47662e-05
PPNAD1 [NCBI] 5.47662e-05
CRH [NCBI] 5.4738e-05
hypertrophic neuropathy of dejerine-sottas [NCBI] 5.45524e-05
mitochondrial myopathy with diabetes [NCBI] 5.15007e-05
EAD [NCBI] 5.15007e-05
sulfocysteinuria [NCBI] 5.15007e-05
weill-marchesani syndrome, autosomal recessive [NCBI] 5.15007e-05
PMD [NCBI] 4.94825e-05
mast cell disease [NCBI] 4.8718e-05
myopathy, myosin storage [NCBI] 4.8718e-05
BCHE [NCBI] 4.77567e-05
INAD1 [NCBI] 4.62964e-05
carnitine palmitoyltransferase ii deficiency, lethal neonatal [NCBI] 4.62964e-05
VDR [NCBI] 4.43414e-05
NETH [NCBI] 4.41549e-05
corneal dystrophy, gelatinous drop-like [NCBI] 4.41549e-05
gaucher disease, perinatal lethal [NCBI] 4.41549e-05
OMP [NCBI] 4.28404e-05
brody myopathy [NCBI] 4.22374e-05
ichthyosis vulgaris [NCBI] 4.22374e-05
LDHC [NCBI] 4.10882e-05
AD [NCBI] 4.10187e-05
F3 [NCBI] 4.08043e-05
mitochondrial dna depletion syndrome, myopathic form [NCBI] 4.05027e-05
MCDC1 [NCBI] 4.05027e-05
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 4.05027e-05
lipoid proteinosis of urbach and wiethe [NCBI] 4.05027e-05
LGMD2H [NCBI] 4.05027e-05
tight skin contracture syndrome, lethal [NCBI] 4.05027e-05
DFSP [NCBI] 4.0163e-05
GNRH1 [NCBI] 3.96618e-05
cutis laxa, autosomal recessive, type i [NCBI] 3.89205e-05
CDGG1 [NCBI] 3.89205e-05
amyloidosis v [NCBI] 3.89205e-05
NCIE1 [NCBI] 3.89205e-05
APC [NCBI] 3.77947e-05
LPG [NCBI] 3.74671e-05
mitochondrial dna depletion syndrome, hepatocerebral form [NCBI] 3.74671e-05
MAG [NCBI] 3.73709e-05
PCNA [NCBI] 3.67061e-05
GAN1 [NCBI] 3.61241e-05
CFTD [NCBI] 3.61241e-05
hypophosphatasia, adult type [NCBI] 3.61241e-05
JH [NCBI] 3.61241e-05
danon disease [NCBI] 3.61241e-05
tibial muscular dystrophy, tardive [NCBI] 3.61241e-05
APOE [NCBI] 3.54788e-05
KLK3 [NCBI] 3.47787e-05
MPO [NCBI] 3.43365e-05
PHA [NCBI] 3.3713e-05
ZS [NCBI] 3.30697e-05
DHFR [NCBI] 3.2972e-05
TNFSF6 [NCBI] 3.2972e-05
BDNF [NCBI] 3.17151e-05
NPHP1 [NCBI] 3.15987e-05
OXT [NCBI] 3.12381e-05
krabbe disease [NCBI] 3.0961e-05
MSS [NCBI] 3.0633e-05
PLOSL [NCBI] 3.0633e-05
MEN2B [NCBI] 3.0633e-05
refsum disease, infantile form [NCBI] 3.0633e-05
TYMS [NCBI] 3.00567e-05
ALD [NCBI] 3.00509e-05
cutis laxa, x-linked [NCBI] 2.97201e-05
CCAL2 [NCBI] 2.97201e-05
hyperoxaluria, primary, type i [NCBI] 2.97201e-05
RTD [NCBI] 2.88549e-05
POMC [NCBI] 2.80619e-05
niemann-pick disease, type a [NCBI] 2.80332e-05
TGD [NCBI] 2.80332e-05
myopathy, myofibrillar, desmin-related [NCBI] 2.72511e-05
LIP [NCBI] 2.72511e-05
EFE [NCBI] 2.72511e-05
PPARA [NCBI] 2.7203e-05
pheochromocytoma [NCBI] 2.5793e-05
PI [NCBI] 2.558e-05
OKS [NCBI] 2.51115e-05
APOB [NCBI] 2.50325e-05
apert syndrome [NCBI] 2.38322e-05
HBB [NCBI] 2.34891e-05
hypophosphatasia, infantile [NCBI] 2.32305e-05
LSA [NCBI] 2.32305e-05
amyloidosis vi [NCBI] 2.30925e-05
DDC [NCBI] 2.223e-05
gastric cancer [NCBI] 2.20947e-05
FLG [NCBI] 2.16784e-05
CAT [NCBI] 2.16527e-05
HPS [NCBI] 2.13962e-05
SJS1 [NCBI] 2.05398e-05
CDPX2 [NCBI] 2.05398e-05
MG [NCBI] 2.01924e-05
NGFR [NCBI] 1.98347e-05
ATS [NCBI] 1.95892e-05
CTNS [NCBI] 1.9137e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 1.9137e-05
HHF1 [NCBI] 1.86989e-05
CDSP [NCBI] 1.78628e-05
SHH [NCBI] 1.77928e-05
CBY [NCBI] 1.75347e-05
MTTA [NCBI] 1.75347e-05
adrenoleukodystrophy, autosomal neonatal form [NCBI] 1.74634e-05
LI1 [NCBI] 1.70756e-05
JPS [NCBI] 1.70756e-05
RBP1 [NCBI] 1.69825e-05
MTCO3 [NCBI] 1.67879e-05
ABL [NCBI] 1.66989e-05
LAD [NCBI] 1.66989e-05
SPARC [NCBI] 1.6548e-05
PWS [NCBI] 1.64583e-05
COMT [NCBI] 1.62039e-05
lymphoma, non-hodgkin, familial [NCBI] 1.60475e-05
SCA6 [NCBI] 1.59769e-05
PYY [NCBI] 1.56773e-05
CMT1B [NCBI] 1.56306e-05
CLIC1 [NCBI] 1.55603e-05
UTS2 [NCBI] 1.55603e-05
ADA [NCBI] 1.54193e-05
BRRS [NCBI] 1.52936e-05
MHS1 [NCBI] 1.46459e-05
FCMD [NCBI] 1.46459e-05
SCA7 [NCBI] 1.43344e-05
LPL [NCBI] 1.41373e-05
LMF1 [NCBI] 1.41042e-05
DNAJB1 [NCBI] 1.41042e-05
PIP5K3 [NCBI] 1.41042e-05
MYH13 [NCBI] 1.41042e-05
KRT3 [NCBI] 1.41042e-05
SFRS2 [NCBI] 1.41042e-05
ST3GAL1 [NCBI] 1.41042e-05
hurler syndrome [NCBI] 1.34461e-05
CJD [NCBI] 1.33715e-05
SLS [NCBI] 1.31644e-05
NGFB [NCBI] 1.31252e-05
polycystic kidneys [NCBI] 1.31147e-05
GAPDH [NCBI] 1.29959e-05
GSCL [NCBI] 1.29535e-05
MPV17 [NCBI] 1.29535e-05
MAK [NCBI] 1.29535e-05
CCBP2 [NCBI] 1.29535e-05
GCM1 [NCBI] 1.29535e-05
ST6GAL1 [NCBI] 1.29535e-05
MAP2 [NCBI] 1.26175e-05
SOD2 [NCBI] 1.24928e-05
glycogen storage disease i [NCBI] 1.24169e-05
GIP [NCBI] 1.20728e-05
SLC6A9 [NCBI] 1.20044e-05
LCP2 [NCBI] 1.20044e-05
TRIM32 [NCBI] 1.11988e-05
ENTPD1 [NCBI] 1.11988e-05
DVL2 [NCBI] 1.11988e-05
GATA6 [NCBI] 1.11988e-05
ZBTB32 [NCBI] 1.11988e-05
MEN2A [NCBI] 1.11347e-05
GDNF [NCBI] 1.10232e-05
LPI [NCBI] 1.09059e-05
metachromatic leukodystrophy [NCBI] 1.06822e-05
CNTF [NCBI] 1.06125e-05
TK2 [NCBI] 1.05003e-05
NEUROG3 [NCBI] 1.05003e-05
MTTE [NCBI] 1.05003e-05
RBL1 [NCBI] 1.05003e-05
menkes disease [NCBI] 1.0249e-05
SHBG [NCBI] 9.88619e-06
DSC1 [NCBI] 9.88508e-06
ATP8B1 [NCBI] 9.88508e-06
PTPRF [NCBI] 9.88508e-06
ACVR1 [NCBI] 9.88508e-06
LEFTY2 [NCBI] 9.88508e-06
SLC30A3 [NCBI] 9.88508e-06
SLC18A3 [NCBI] 9.56856e-06
SI [NCBI] 9.56592e-06
thrombocytopenic purpura, autoimmune [NCBI] 9.49281e-06
TG [NCBI] 9.4366e-06
DAO [NCBI] 9.34429e-06
RTN1 [NCBI] 9.33632e-06
FABP7 [NCBI] 9.33632e-06
osteogenesis imperfecta, type i [NCBI] 9.05419e-06
SMARCA4 [NCBI] 8.84189e-06
MEIS1 [NCBI] 8.84189e-06
PITX3 [NCBI] 8.84189e-06
SMA1 [NCBI] 8.68763e-06
TFPI2 [NCBI] 8.65101e-06
ZNF198 [NCBI] 8.3927e-06
KRT8 [NCBI] 8.3927e-06
PITX1 [NCBI] 8.3927e-06
IDH1 [NCBI] 8.3927e-06
GDF11 [NCBI] 8.3927e-06
PPY [NCBI] 8.3927e-06
SRF [NCBI] 8.12116e-06
CGD [NCBI] 7.99711e-06
NAGA [NCBI] 7.98177e-06
SDHC [NCBI] 7.98177e-06
TFF2 [NCBI] 7.98177e-06
MFS [NCBI] 7.93636e-06
SPINK1 [NCBI] 7.7693e-06
GRP [NCBI] 7.72965e-06
MB [NCBI] 7.7108e-06
wilson disease [NCBI] 7.67172e-06
CGA [NCBI] 7.60362e-06
SORBS1 [NCBI] 7.60362e-06
panencephalitis, subacute sclerosing [NCBI] 7.47927e-06
MMP13 [NCBI] 7.25388e-06
HD [NCBI] 7.17863e-06
LAMP2 [NCBI] 6.92897e-06
BAK1 [NCBI] 6.92897e-06
EN1 [NCBI] 6.62597e-06
THY1 [NCBI] 6.62597e-06
PTH [NCBI] 6.4849e-06
TNFRSF11B [NCBI] 6.36581e-06
P4HB [NCBI] 6.34245e-06
PAPPA [NCBI] 6.34245e-06
FGF9 [NCBI] 6.07636e-06
HMOX1 [NCBI] 6.07636e-06
DBI [NCBI] 6.07291e-06
IL3 [NCBI] 6.07066e-06
CDLS1 [NCBI] 5.95989e-06
tay-sachs disease, ab variant [NCBI] 5.82594e-06
CEACAM6 [NCBI] 5.82594e-06
BMP2 [NCBI] 5.641e-06
UGB [NCBI] 5.641e-06
NRL [NCBI] 5.5897e-06
RNASE3 [NCBI] 5.51748e-06
PDGFRA [NCBI] 5.36635e-06
AMPD1 [NCBI] 5.36635e-06
SLC5A5 [NCBI] 5.36635e-06
CYP27B1 [NCBI] 5.36635e-06
PDGFRB [NCBI] 5.36635e-06
NKX2-1 [NCBI] 5.15477e-06
SLC5A7 [NCBI] 5.15477e-06
OSM [NCBI] 5.03462e-06
MAPK8 [NCBI] 4.95398e-06
MAP2K1 [NCBI] 4.95398e-06
SLC17A6 [NCBI] 4.95398e-06
SDC2 [NCBI] 4.94911e-06
TGM1 [NCBI] 4.76312e-06
CCK [NCBI] 4.71325e-06
ABP1 [NCBI] 4.59699e-06
GJA1 [NCBI] 4.48308e-06
ichthyosis, x-linked [NCBI] 4.44135e-06
MLP [NCBI] 4.40819e-06
NOS1 [NCBI] 4.40819e-06
BWS [NCBI] 4.20237e-06
PITX2 [NCBI] 4.08482e-06
CALCA [NCBI] 4.08482e-06
INS [NCBI] 4.06499e-06
EV [NCBI] 4.00597e-06
CHGA [NCBI] 3.93365e-06
TTR [NCBI] 3.89714e-06
ADH5 [NCBI] 3.78888e-06
CST3 [NCBI] 3.78888e-06
HDC [NCBI] 3.77462e-06
CTGF [NCBI] 3.77028e-06
CP [NCBI] 3.71488e-06
glycogen storage disease ixa [NCBI] 3.6501e-06
DCN [NCBI] 3.6501e-06
COL10A1 [NCBI] 3.51697e-06
VIM [NCBI] 3.48174e-06
MBP [NCBI] 3.37459e-06
TF [NCBI] 3.24683e-06
PG [NCBI] 3.22553e-06
FGF7 [NCBI] 3.16586e-06
OA1 [NCBI] 3.1482e-06
aspartylglucosaminuria [NCBI] 3.1482e-06
ICAM1 [NCBI] 3.1482e-06
IL13 [NCBI] 3.1482e-06
NR6A1 [NCBI] 3.03456e-06
BAX [NCBI] 2.92516e-06
ADRP [NCBI] 2.92516e-06
TPI1 [NCBI] 2.81977e-06
fucosidosis [NCBI] 2.62025e-06
RP [NCBI] 2.44492e-06
ARF6 [NCBI] 2.43457e-06
GHR [NCBI] 2.40346e-06
CDK2 [NCBI] 2.37788e-06
HEXB [NCBI] 2.34652e-06
BRAF [NCBI] 2.34652e-06
RUNX1 [NCBI] 2.17932e-06
FGFR3 [NCBI] 2.12643e-06
SERPINA6 [NCBI] 2.05264e-06
APCS [NCBI] 2.02313e-06
HCRT [NCBI] 1.87706e-06
COL3A1 [NCBI] 1.87706e-06
AANAT [NCBI] 1.87706e-06
PGR [NCBI] 1.74101e-06
XDH [NCBI] 1.58471e-06
MYH7 [NCBI] 1.4922e-06
OTC [NCBI] 1.4922e-06
PTHLH [NCBI] 1.43619e-06
PLP1 [NCBI] 1.435e-06
GHRH [NCBI] 1.40276e-06
GNRHR [NCBI] 1.3796e-06
AKR1B1 [NCBI] 1.32777e-06
SPP1 [NCBI] 1.31837e-06
CDH1 [NCBI] 1.22361e-06
ASL [NCBI] 1.22361e-06
MMP9 [NCBI] 1.22361e-06
TPO [NCBI] 1.21336e-06
MMP2 [NCBI] 1.08179e-06
DNTT [NCBI] 1.03744e-06
ADCYAP1 [NCBI] 1.00383e-06
FOXP3 [NCBI] 9.94473e-07
PJS [NCBI] 9.62326e-07
NMU [NCBI] 9.52856e-07
TGFB1 [NCBI] 9.52856e-07
CD [NCBI] 9.1721e-07
GPT [NCBI] 9.12544e-07
AVP [NCBI] 8.61143e-07
TFF3 [NCBI] 8.3569e-07
DSPP [NCBI] 8.3569e-07
SST [NCBI] 7.35355e-07
DGS [NCBI] 5.99646e-07
HFE [NCBI] 5.85122e-07
DMD [NCBI] 5.48913e-07
ACE [NCBI] 4.87481e-07
IHH [NCBI] 4.5025e-07
BSG [NCBI] 4.42236e-07
PF4 [NCBI] 4.40892e-07
APP [NCBI] 4.19712e-07
ASS [NCBI] 3.73791e-07
CLU [NCBI] 3.73791e-07
PRL [NCBI] 3.71192e-07
mucopolysaccharidosis type ii [NCBI] 2.57918e-07
FGFR2 [NCBI] 2.53344e-07
CPI [NCBI] 2.32239e-07
TERT [NCBI] 1.98734e-07
homocystinuria [NCBI] 1.94803e-07
GIST [NCBI] 1.89222e-07
CVID [NCBI] 1.62408e-07
NPPA [NCBI] 1.61144e-07
PAEP [NCBI] 1.30207e-07
BL [NCBI] 1.28074e-07
PMCH [NCBI] 1.11522e-07
TS [NCBI] 9.25912e-08
GUSB [NCBI] 7.16582e-08
ALB [NCBI] 6.70093e-08
AMH [NCBI] 5.02591e-08
KDR [NCBI] 3.62928e-08
PCI [NCBI] 3.16795e-08
dystrophia myotonica 1 [NCBI] 1.79598e-08
FGFR1 [NCBI] 1.58924e-08
MJD [NCBI] 1.46989e-08
RNASE2 [NCBI] 8.35723e-09
UCN [NCBI] 3.99549e-09
BCR [NCBI] 2.49496e-09
LPO [NCBI] 2.42283e-09
PKD1 [NCBI] 1.24684e-09
GJB1 [NCBI] 1.24684e-09
UCP2 [NCBI] 1.24684e-09
CCND1 [NCBI] 3.84023e-10




Database Center for Life Science