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01 Ear, External [NCBI]


Gene


Gene Link Information
Gain
01
HFM [NCBI] 0.00389007
PAFC [NCBI] 0.000392232
VCF [NCBI] 0.000275593
MS [NCBI] 4.68154e-05
SALL1 [NCBI] 4.35769e-05
EYA1 [NCBI] 1.91185e-05
TFPI [NCBI] 8.27012e-06
BMP7 [NCBI] 7.28145e-06
IL18BP [NCBI] 6.69623e-06
CHD8 [NCBI] 6.53566e-06
KRT3 [NCBI] 5.93916e-06
SUPT16H [NCBI] 5.93916e-06
NPY [NCBI] 5.79368e-06
TCOF1 [NCBI] 5.6262e-06
BMP2 [NCBI] 5.32726e-06
IL17RA [NCBI] 5.25626e-06
FGF3 [NCBI] 4.70175e-06
RPS19 [NCBI] 4.61149e-06
KRT5 [NCBI] 4.57965e-06
MEF2C [NCBI] 4.57965e-06
FGF10 [NCBI] 4.48032e-06
VEGFA [NCBI] 4.24086e-06
HGF [NCBI] 4.2238e-06
TWIST1 [NCBI] 4.16688e-06
MPO [NCBI] 4.16572e-06
CYSLTR2 [NCBI] 4.14642e-06
FPR2 [NCBI] 4.11324e-06
CD79A [NCBI] 3.99642e-06
PLG [NCBI] 3.97917e-06
PCNA [NCBI] 3.96084e-06
CD40 [NCBI] 3.82151e-06
EGF [NCBI] 3.44232e-06
SOX9 [NCBI] 3.41714e-06
DCT [NCBI] 3.35483e-06
NME1 [NCBI] 3.28778e-06
INS [NCBI] 3.28497e-06
MATN1 [NCBI] 3.25727e-06
FGF7 [NCBI] 3.12238e-06
FMR1 [NCBI] 3.06473e-06
SELPLG [NCBI] 3.0536e-06
GJB2 [NCBI] 2.98732e-06
PROM1 [NCBI] 2.89105e-06
CDK4 [NCBI] 2.49329e-06
CDK2 [NCBI] 1.98734e-06
LIF [NCBI] 1.83675e-06
TNF [NCBI] 1.70877e-06
MBP [NCBI] 1.53122e-06
TGFB1 [NCBI] 1.42822e-06
PTGS2 [NCBI] 1.1064e-06
TH [NCBI] 1.02027e-06
CASP3 [NCBI] 7.54096e-07




OMIM


OMIM Link Information
gain
01
HFM [NCBI] 0.00941662
microtia with meatal atresia and conductive deafness [NCBI] 0.00655293
microtia-anotia [NCBI] 0.00618408
auriculocondylar syndrome [NCBI] 0.0039641
hypertelorism, microtia, facial clefting syndrome [NCBI] 0.00257433
preauricular fistulae, congenital [NCBI] 0.00232632
aural atresia, congenital [NCBI] 0.00204776
TBS [NCBI] 0.00165039
earlobes, thickened, with conductive deafness from incudostapedial abnormalities [NCBI] 0.0016217
preauricular tag, isolated, autosomal dominant, 1 [NCBI] 0.00102222
diamond-blackfan anemia with microtia and cleft palate [NCBI] 0.00102222
actinic prurigo [NCBI] 0.00102222
ear malformation [NCBI] 0.00102222
ear, patella, short stature syndrome [NCBI] 0.000898584
marden-walker syndrome [NCBI] 0.000898584
earlobe crease [NCBI] 0.000870111
LADD [NCBI] 0.000830476
charge syndrome [NCBI] 0.000801044
hairy ears, y-linked [NCBI] 0.000793577
kabuki syndrome [NCBI] 0.000727254
deafness, conductive, with malformed external ear [NCBI] 0.000713579
otoonychoperoneal syndrome [NCBI] 0.000713579
BOR1 [NCBI] 0.000634027
nablus mask-like facial syndrome [NCBI] 0.000598547
hypoadrenocorticism, familial [NCBI] 0.000598547
branchiootic syndrome 2 [NCBI] 0.000524669
pena-shokeir syndrome, type i [NCBI] 0.000477757
hemifacial microsomia with radial defects [NCBI] 0.000470337
hairy ears [NCBI] 0.000457622
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.000427518
dermatitis, atopic [NCBI] 0.000427518
skin creases, multiple benign ring-shaped, of limbs [NCBI] 0.0003625
earlobe attachment: attached vs unattached [NCBI] 0.000347271
ZLS [NCBI] 0.000336737
AMCN [NCBI] 0.000336737
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.000336737
MCOPS1 [NCBI] 0.000336737
BOS1 [NCBI] 0.000330649
charge-like syndrome, x-linked [NCBI] 0.00029323
ear pits, posterior helical [NCBI] 0.00029323
CES [NCBI] 0.000282571
isotretinoin embryopathy-like syndrome [NCBI] 0.000268839
say syndrome [NCBI] 0.000268839
SLE [NCBI] 0.000194909
RA [NCBI] 0.000193733
SALL1 [NCBI] 0.000189115
contractural arachnodactyly, congenital [NCBI] 0.000174837
NHS [NCBI] 0.00017373
ossified ear cartilages [NCBI] 0.000173508
arthrogryposis, distal, type 2e [NCBI] 0.000173508
speech development, delayed, with facial asymmetry, strabismus, and transverse earlobe crease [NCBI] 0.000173508
simosa craniofacial syndrome [NCBI] 0.000173508
cryptotia, familial [NCBI] 0.000173508
ear folding [NCBI] 0.000173508
aurocephalosyndactyly [NCBI] 0.000173508
deafness, conductive stapedial, with ear malformation and facial palsy [NCBI] 0.000173508
ossified ear cartilages with mental deficiency, muscle wasting, and bony changes [NCBI] 0.000173508
microcephaly-cardiomyopathy [NCBI] 0.000173508
ABS [NCBI] 0.000170352
BWS [NCBI] 0.000147838
phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia [NCBI] 0.000134293
mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia [NCBI] 0.000134293
radial-renal syndrome [NCBI] 0.000134293
OAFNS [NCBI] 0.000134293
deafness, congenital, with inner ear agenesis, microtia, and microdontia [NCBI] 0.000134293
creases, infra-auricular cutaneous, with tall stature and advanced bone age [NCBI] 0.000134293
split-foot deformity with mandibulofacial dysostosis [NCBI] 0.00011953
brachycephaly, deafness, cataract, microstomia, and mental retardation [NCBI] 0.00011953
EEC1 [NCBI] 0.000117993
native american myopathy [NCBI] 0.000109964
intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies [NCBI] 0.000109964
mental retardation, fra12a type [NCBI] 0.000102867
scalp-ear-nipple syndrome [NCBI] 0.000102867
poland syndrome [NCBI] 0.000101844
NHS [NCBI] 9.88362e-05
palatopharyngeal incompetence [NCBI] 9.69674e-05
tetralogy of fallot [NCBI] 8.8542e-05
rokitansky-kuster-hauser syndrome [NCBI] 8.19603e-05
corpus callosum, agenesis of [NCBI] 7.91841e-05
ACG2 [NCBI] 7.91841e-05
ALSG [NCBI] 7.66667e-05
hypertelorism with esophageal abnormality and hypospadias [NCBI] 7.57259e-05
OPD2 [NCBI] 7.2245e-05
COFS1 [NCBI] 7.2245e-05
GACI [NCBI] 6.8453e-05
pfeiffer syndrome [NCBI] 6.67429e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 6.51372e-05
AFD1 [NCBI] 6.36242e-05
SGBS1 [NCBI] 5.60352e-05
AHC [NCBI] 5.01993e-05
DGS [NCBI] 5.00597e-05
SCS [NCBI] 4.62073e-05
CCM [NCBI] 4.34296e-05
MATN1 [NCBI] 4.1979e-05
GPRK6 [NCBI] 4.1979e-05
ALGS1 [NCBI] 3.8699e-05
LYZ [NCBI] 3.73219e-05
TFPI [NCBI] 3.68549e-05
SMAD3 [NCBI] 3.50017e-05
CDLS1 [NCBI] 3.07091e-05
DBA [NCBI] 2.82657e-05
FGF10 [NCBI] 2.81898e-05
WHS [NCBI] 2.41303e-05
FGF1 [NCBI] 2.19978e-05
fragile x mental retardation syndrome [NCBI] 2.16501e-05
PLG [NCBI] 2.07692e-05
krabbe disease [NCBI] 1.9476e-05
CDK4 [NCBI] 1.87719e-05
INS [NCBI] 1.5595e-05
CDK2 [NCBI] 1.53827e-05
GJA1 [NCBI] 1.25713e-05
NPY [NCBI] 1.20158e-05
HGF [NCBI] 1.05964e-05
FGF7 [NCBI] 1.0336e-05
VEGF [NCBI] 9.8518e-06
MPO [NCBI] 9.7517e-06
PCNA [NCBI] 8.85139e-06
MBP [NCBI] 2.05694e-06
EGF [NCBI] 1.59332e-06
TH [NCBI] 2.27869e-07
TNF [NCBI] 1.53229e-07
SRS [NCBI] 3.22056e-08




Database Center for Life Science