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01 Cytogenetics [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
3-@hydroxyisobutyric aciduria [NCBI] 0.00132272
neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers [NCBI] 0.000957753
cutis laxa, corneal clouding, and mental retardation [NCBI] 0.000892923
x inactivation, familial skewed, 2 [NCBI] 0.000844761
ASD1 [NCBI] 0.00077456
IH [NCBI] 0.00077456
ST3 [NCBI] 0.0005482
lipomatosis, multiple [NCBI] 0.000516265
fragile x mental retardation syndrome [NCBI] 0.000249916
peroxidase and phospholipid deficiency in eosinophils [NCBI] 0.000199809
nondisjunction [NCBI] 0.000158497
dohle bodies and leukemia [NCBI] 0.000137984
myelocytic leukemia-like syndrome, familial, chronic [NCBI] 0.000110231
acrofacial dysostosis, catania type [NCBI] 0.000110231
CES [NCBI] 0.000101728
MRX58 [NCBI] 9.97678e-05
yemenite deaf-blind hypopigmentation syndrome [NCBI] 9.97678e-05
FA [NCBI] 8.82345e-05
LVNC1 [NCBI] 8.79385e-05
POF2A [NCBI] 8.79385e-05
erythroleukemia, familial [NCBI] 8.39247e-05
thyrotropin deficiency, isolated [NCBI] 8.39247e-05
frontonasal dysplasia [NCBI] 8.05903e-05
PWS [NCBI] 7.91233e-05
SMS [NCBI] 7.81349e-05
ODG2 [NCBI] 7.77387e-05
dyskeratosis congenita, autosomal dominant [NCBI] 7.52482e-05
currarino syndrome [NCBI] 7.52482e-05
ADHR [NCBI] 7.52482e-05
monosomy 7 of bone marrow [NCBI] 7.30378e-05
chromosome 18q deletion syndrome [NCBI] 6.75966e-05
chromosome 22q13.3 deletion syndrome [NCBI] 6.75966e-05
potocki-shaffer syndrome [NCBI] 6.46624e-05
CF [NCBI] 6.40777e-05
exostoses, multiple, type ii [NCBI] 6.3346e-05
infantile spasm syndrome, x-linked [NCBI] 6.21134e-05
MVA [NCBI] 6.21134e-05
BGS [NCBI] 6.09545e-05
OCRL [NCBI] 5.43544e-05
neural tube defects [NCBI] 5.21008e-05
POF1 [NCBI] 5.21008e-05
testicular tumors [NCBI] 5.14055e-05
apert syndrome [NCBI] 5.14055e-05
hypophosphatasia, infantile [NCBI] 5.07348e-05
deleted in neuroblastoma 5 [NCBI] 4.91634e-05
meningioma, familial [NCBI] 4.76994e-05
MDLS [NCBI] 4.71472e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 4.50894e-05
RSTS [NCBI] 4.46088e-05
SCS [NCBI] 4.2803e-05
sotos syndrome [NCBI] 4.2803e-05
down syndrome [NCBI] 4.11598e-05
RERE [NCBI] 4.09172e-05
CENTA2 [NCBI] 4.09172e-05
AN2 [NCBI] 4.07712e-05
RDT [NCBI] 3.76073e-05
prostate cancer [NCBI] 3.7288e-05
MUC1 [NCBI] 3.7164e-05
porphyria variegata [NCBI] 3.66663e-05
velocardiofacial syndrome [NCBI] 3.60658e-05
MKRN1 [NCBI] 3.57857e-05
CMT1A [NCBI] 3.54852e-05
lynch syndrome i [NCBI] 3.38513e-05
NS1 [NCBI] 3.25987e-05
TM4SF2 [NCBI] 3.12415e-05
MAS [NCBI] 3.07688e-05
PEPB [NCBI] 3.04974e-05
ARD1A [NCBI] 3.04974e-05
danubian endemic familial nephropathy [NCBI] 3.03408e-05
BBS4 [NCBI] 2.98365e-05
MIRN155 [NCBI] 2.98365e-05
AL-A1 [NCBI] 2.8702e-05
MSN [NCBI] 2.82072e-05
ZNF198 [NCBI] 2.82072e-05
IDH1 [NCBI] 2.82072e-05
CD14 [NCBI] 2.73268e-05
HEPH [NCBI] 2.69314e-05
UBE1 [NCBI] 2.69314e-05
CCKAR [NCBI] 2.69314e-05
CNR1 [NCBI] 2.65609e-05
DDR1 [NCBI] 2.62122e-05
EV [NCBI] 2.59232e-05
IL9 [NCBI] 2.55713e-05
FRAXE [NCBI] 2.55713e-05
BBS [NCBI] 2.4986e-05
TK1 [NCBI] 2.42207e-05
BCNS [NCBI] 2.4102e-05
NKX2E [NCBI] 2.39842e-05
LDHB [NCBI] 2.37568e-05
CDKN1B [NCBI] 2.25516e-05
SKP2 [NCBI] 2.25516e-05
MN [NCBI] 2.23728e-05
SOX10 [NCBI] 2.21993e-05
PPOX [NCBI] 2.20308e-05
PHEX [NCBI] 2.17077e-05
XPA [NCBI] 2.15527e-05
SHOX [NCBI] 2.14016e-05
EGR1 [NCBI] 2.09707e-05
CSF2 [NCBI] 2.09707e-05
DFSP [NCBI] 1.92552e-05
DCC [NCBI] 1.9094e-05
SPARC [NCBI] 1.83436e-05
DGS [NCBI] 1.8167e-05
lymphoma, non-hodgkin, familial [NCBI] 1.81181e-05
IL3 [NCBI] 1.76021e-05
PAX6 [NCBI] 1.75253e-05
CPI [NCBI] 1.65561e-05
COL2A1 [NCBI] 1.63573e-05
GCK [NCBI] 1.62344e-05
FGF1 [NCBI] 1.6174e-05
IL4 [NCBI] 1.58242e-05
SRY [NCBI] 1.57123e-05
KRT20 [NCBI] 1.57123e-05
NPM1 [NCBI] 1.47942e-05
HPRT1 [NCBI] 1.47942e-05
FGFR1 [NCBI] 1.42139e-05
apc gene [NCBI] 1.27684e-05
DCK [NCBI] 1.18154e-05
phenylketonuria [NCBI] 1.12221e-05
BWS [NCBI] 1.10871e-05
BCR [NCBI] 1.08003e-05
APRT [NCBI] 1.0711e-05
SOD1 [NCBI] 1.01653e-05
AS [NCBI] 8.82705e-06
AD [NCBI] 8.13124e-06
CAT [NCBI] 7.71334e-06
HP [NCBI] 7.31824e-06
AR [NCBI] 5.17762e-06
FRAP1 [NCBI] 5.11733e-06
POMC [NCBI] 4.85993e-06
CRC [NCBI] 4.80604e-06
EGF [NCBI] 4.12503e-06
SHH [NCBI] 3.78754e-06
TYMS [NCBI] 3.52977e-06
TNF [NCBI] 3.23474e-06
G6PD [NCBI] 2.68708e-06
F3 [NCBI] 1.81638e-06
AFP [NCBI] 7.20072e-07
MPO [NCBI] 6.10129e-07
APOE [NCBI] 6.08173e-07
thrombocytopenic purpura, autoimmune [NCBI] 2.47386e-07
EPO [NCBI] 1.39758e-07
KLK3 [NCBI] 4.10453e-09
APC [NCBI] 4.77738e-11



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