Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ear Canal [NCBI]

Gene


 Gene Link Information
Gain		 01
HFM [NCBI] 0.000347245
CTNNB1 [NCBI] 1.52878e-05
POU3F4 [NCBI] 1.52428e-05
SLC26A2 [NCBI] 1.36723e-05
DEFB1 [NCBI] 1.14305e-05
LGALS8 [NCBI] 6.4397e-06
S100A1 [NCBI] 6.4397e-06
VEGFA [NCBI] 5.83973e-06
HGF [NCBI] 5.82221e-06
TGFB1 [NCBI] 5.76088e-06
RPS19 [NCBI] 5.42368e-06
KRT7 [NCBI] 4.45302e-06
DEFB4 [NCBI] 4.3486e-06
MUC1 [NCBI] 4.03099e-06
VHL [NCBI] 3.83368e-06
GJB2 [NCBI] 3.791e-06
PTHLH [NCBI] 3.38325e-06
BMP2 [NCBI] 2.77188e-06
HIF1A [NCBI] 2.55068e-06
BCL2L1 [NCBI] 2.48947e-06
VWF [NCBI] 2.44487e-06
PCNA [NCBI] 2.08598e-06
PTH [NCBI] 1.75196e-06
PRL [NCBI] 1.65857e-06



OMIM


 OMIM Link Information
gain		 01
microtia with meatal atresia and conductive deafness [NCBI] 0.00346126
aural atresia, congenital [NCBI] 0.00120455
atresia of external auditory canal and conduction deafness [NCBI] 0.00120455
HFM [NCBI] 0.00114649
microtia-anotia [NCBI] 0.000910064
proteus syndrome [NCBI] 0.000618297
external auditory canal, bilateral atresia of, with congenital vertical talus [NCBI] 0.000496453
short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities [NCBI] 0.000496453
aural atresia, multiple congenital anomalies, and mental retardation [NCBI] 0.000246451
rokitansky-kuster-hauser syndrome [NCBI] 0.000154387
NF2 [NCBI] 0.000123333
walker-warburg syndrome [NCBI] 0.000117141
DBA [NCBI] 9.70746e-05
POU3F4 [NCBI] 4.86251e-05
GJA1 [NCBI] 2.41406e-05
VEGF [NCBI] 1.58597e-05
KLK3 [NCBI] 1.37875e-05
HGF [NCBI] 1.121e-05
PCNA [NCBI] 1.01699e-05
PTH [NCBI] 7.82821e-06
PRL [NCBI] 7.14596e-06



Database Center for Life Science