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MeSH keywords -> Related genes, diseases (OMIM)


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01 Respiratory Insufficiency [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.000253419
IGHMBP2 [NCBI] 4.22849e-05
GER [NCBI] 3.4922e-05
CALCA [NCBI] 3.03876e-05
SFTPB [NCBI] 2.79233e-05
ABCA3 [NCBI] 2.72126e-05
FKRP [NCBI] 2.64914e-05
GAA [NCBI] 2.33039e-05
MUSK [NCBI] 2.20322e-05
TTN [NCBI] 1.84739e-05
NKX2-1 [NCBI] 1.67254e-05
TRIM55 [NCBI] 1.54743e-05
SYNC [NCBI] 1.08332e-05
SMN1 [NCBI] 1.07277e-05
LAMP3 [NCBI] 1.00849e-05
TNF [NCBI] 9.91262e-06
SLC25A20 [NCBI] 9.89391e-06
PBX3 [NCBI] 9.42294e-06
SGCA [NCBI] 9.29093e-06
MTNR1A [NCBI] 9.29093e-06
TF [NCBI] 9.22992e-06
PRKCH [NCBI] 9.16838e-06
TPM2 [NCBI] 9.05403e-06
MAN1C1 [NCBI] 8.66053e-06
MUC1 [NCBI] 8.54091e-06
SEPN1 [NCBI] 8.34091e-06
TCAP [NCBI] 8.26955e-06
PTGER3 [NCBI] 8.1352e-06
ALMS1 [NCBI] 8.07179e-06
NBR1 [NCBI] 7.73411e-06
HSD17B4 [NCBI] 7.68381e-06
SFTPC [NCBI] 7.32735e-06
PRKCZ [NCBI] 7.28762e-06
SBDS [NCBI] 7.2488e-06
LTBR [NCBI] 7.2488e-06
ABCG8 [NCBI] 7.17372e-06
ELAVL4 [NCBI] 6.90278e-06
PKHD1 [NCBI] 6.78199e-06
ALPL [NCBI] 6.61558e-06
FKTN [NCBI] 6.58937e-06
CRYAB [NCBI] 6.48841e-06
SQSTM1 [NCBI] 6.32508e-06
CFTR [NCBI] 6.20724e-06
PHOX2B [NCBI] 5.89562e-06
PHEX [NCBI] 5.79533e-06
MYH7 [NCBI] 5.65534e-06
ACHE [NCBI] 5.59695e-06
AVP [NCBI] 5.52859e-06
CD40 [NCBI] 5.39352e-06
TSC2 [NCBI] 5.27066e-06
IL13 [NCBI] 4.85416e-06
SMN2 [NCBI] 4.79099e-06
CYP2D6 [NCBI] 4.78216e-06
LTA [NCBI] 4.22776e-06
SCGB1A1 [NCBI] 4.12473e-06
OSM [NCBI] 4.03347e-06
DMPK [NCBI] 3.86029e-06
PTPN11 [NCBI] 3.81135e-06
PRKCA [NCBI] 3.79695e-06
GAPDH [NCBI] 3.76855e-06
MPO [NCBI] 3.7505e-06
PF4 [NCBI] 3.69077e-06
ALK [NCBI] 3.6252e-06
TPO [NCBI] 3.54592e-06
PIH [NCBI] 3.5018e-06
CCR2 [NCBI] 3.34406e-06
ADIPOQ [NCBI] 3.32632e-06
IL8 [NCBI] 3.12499e-06
MAPT [NCBI] 2.98073e-06
SHBG [NCBI] 2.82629e-06
CHAT [NCBI] 2.80371e-06
NOD2 [NCBI] 2.66833e-06
IL1B [NCBI] 2.50562e-06
CST3 [NCBI] 2.4327e-06
VIP [NCBI] 2.17905e-06
ACE [NCBI] 2.00853e-06
TLR4 [NCBI] 1.96169e-06
SOD1 [NCBI] 1.93623e-06
BDNF [NCBI] 1.83431e-06
TH [NCBI] 1.77107e-06
IL1RN [NCBI] 1.45312e-06
HGF [NCBI] 1.37754e-06
TGFB1 [NCBI] 1.08201e-06
GFAP [NCBI] 1.00484e-06
EPO [NCBI] 9.44315e-07
AFP [NCBI] 8.98789e-07
PRL [NCBI] 7.78367e-07
EGFR [NCBI] 3.4549e-07




OMIM


OMIM Link Information
gain
01
ATD1 [NCBI] 0.00291706
adducted thumbs syndrome [NCBI] 0.000714407
spondylometaphyseal dysplasia, sedaghatian type [NCBI] 0.000621736
pierre robin sequence with pectus excavatum and rib and scapular anomalies [NCBI] 0.000590318
FSHMD1A [NCBI] 0.000532147
glycogen storage disease ii [NCBI] 0.000492588
myeloproliferative syndrome, transient [NCBI] 0.000321967
poland syndrome [NCBI] 0.00031277
CF [NCBI] 0.000294654
stuve-wiedemann syndrome [NCBI] 0.000288302
HMERF [NCBI] 0.000285163
RSMD1 [NCBI] 0.000228106
RA [NCBI] 0.000190178
MG [NCBI] 0.000156268
LGMD2I [NCBI] 0.000124031
SLE [NCBI] 0.000120374
myopathy, distal, with early respiratory failure, autosomal dominant [NCBI] 0.000107066
obesity-hypoventilation syndrome [NCBI] 0.000107066
SFTPB [NCBI] 0.000101864
myopathy, myofibrillar, desmin-related [NCBI] 9.92378e-05
TTN [NCBI] 9.1011e-05
SJS1 [NCBI] 8.18596e-05
NEM3 [NCBI] 8.11686e-05
IL13 [NCBI] 8.06917e-05
LAM [NCBI] 7.63559e-05
larsen-like syndrome, lethal type [NCBI] 7.61552e-05
respiratory underresponsiveness to hypoxia and hypercapnia [NCBI] 7.61552e-05
sickle cell anemia [NCBI] 7.50072e-05
apnea, obstructive sleep [NCBI] 7.1995e-05
aminopterin syndrome sine aminopterin [NCBI] 7.06687e-05
TLPD [NCBI] 7.06687e-05
immunodeficiency with hyper-igm, type 3 [NCBI] 6.65946e-05
NBR1 [NCBI] 6.39235e-05
choreoathetosis, hypothyroidism, and neonatal respiratory distress [NCBI] 6.33524e-05
creatine phosphokinase, elevated serum [NCBI] 6.33524e-05
RTT [NCBI] 6.33209e-05
IL11 [NCBI] 5.8726e-05
IL11RA [NCBI] 5.8726e-05
MDC1C [NCBI] 5.8358e-05
AVP [NCBI] 5.59721e-05
lenz-majewski hyperostotic dwarfism [NCBI] 5.45652e-05
leiomyomatosis, esophageal and vulval, with nephropathy [NCBI] 5.29633e-05
SMDP1 [NCBI] 5.15095e-05
CSF2RB [NCBI] 5.08467e-05
SEPN1 [NCBI] 4.91861e-05
multiple pterygium syndrome, escobar variant [NCBI] 4.78155e-05
cerebrocostomandibular syndrome [NCBI] 4.78155e-05
JMJD6 [NCBI] 4.77651e-05
CD40 [NCBI] 4.65233e-05
HSD17B4 [NCBI] 4.65233e-05
CFTD [NCBI] 4.5764e-05
myasthenic syndrome, congenital, associated with episodic apnea [NCBI] 4.5764e-05
FMD [NCBI] 4.48317e-05
KSS [NCBI] 4.47169e-05
NDN [NCBI] 4.27023e-05
RTD [NCBI] 4.23319e-05
MMP12 [NCBI] 4.19409e-05
NKX2-1 [NCBI] 4.12342e-05
GACI [NCBI] 4.08663e-05
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 4.01831e-05
HSS [NCBI] 4.01831e-05
PTPRC [NCBI] 3.88275e-05
NOS2A [NCBI] 3.88275e-05
sudden infant death syndrome [NCBI] 3.83009e-05
EDN1 [NCBI] 3.68972e-05
citrullinemia, classic [NCBI] 3.66278e-05
leopard syndrome 1 [NCBI] 3.61093e-05
IL8 [NCBI] 3.56647e-05
niemann-pick disease, type a [NCBI] 3.56081e-05
SCDO1 [NCBI] 3.51233e-05
FKRP [NCBI] 3.4922e-05
SEDC [NCBI] 3.33291e-05
TF [NCBI] 3.29999e-05
GAA [NCBI] 3.26953e-05
LIP [NCBI] 3.17308e-05
campomelic dysplasia [NCBI] 3.09932e-05
MMP9 [NCBI] 2.95681e-05
MYH7 [NCBI] 2.87802e-05
FCMD [NCBI] 2.66837e-05
PWS [NCBI] 2.38437e-05
LPI [NCBI] 2.22087e-05
MAPT [NCBI] 2.134e-05
MECP2 [NCBI] 1.9997e-05
LS [NCBI] 1.94803e-05
RNASE3 [NCBI] 1.85944e-05
NPPA [NCBI] 1.82509e-05
OSM [NCBI] 1.7685e-05
ACH [NCBI] 1.58067e-05
TNF [NCBI] 1.482e-05
PI [NCBI] 1.33283e-05
CMH [NCBI] 1.27746e-05
ACHE [NCBI] 1.21746e-05
NF1 [NCBI] 1.15418e-05
GAPDH [NCBI] 1.14625e-05
PF4 [NCBI] 1.08814e-05
VEGF [NCBI] 1.01565e-05
dystrophia myotonica 1 [NCBI] 7.51198e-06
MFS [NCBI] 6.7503e-06
SHBG [NCBI] 6.2924e-06
CHAT [NCBI] 6.17363e-06
MUC1 [NCBI] 4.9604e-06
MPO [NCBI] 4.81544e-06
VIP [NCBI] 3.38994e-06
F3 [NCBI] 2.98017e-06
CFTR [NCBI] 2.50707e-06
BDNF [NCBI] 2.33239e-06
TH [NCBI] 1.74239e-06
CEACAM5 [NCBI] 1.51923e-06
HGF [NCBI] 9.82578e-07
GFAP [NCBI] 7.50801e-08
PRL [NCBI] 4.8319e-08
EPO [NCBI] 3.52741e-08
AFP [NCBI] 1.39197e-08




Database Center for Life Science