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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hearing Loss, Conductive [NCBI]


Gene


Gene Link Information
Gain
01
OTSC1 [NCBI] 0.000381162
OTSC4 [NCBI] 0.000381162
FOP [NCBI] 0.000376119
OSCS [NCBI] 0.000320423
HFM [NCBI] 0.000173325
NOG [NCBI] 9.26065e-05
POU3F4 [NCBI] 2.47719e-05
SOST [NCBI] 2.35647e-05
GJB2 [NCBI] 2.12124e-05
COL2A1 [NCBI] 1.75461e-05
SIX1 [NCBI] 1.06548e-05
USH1C [NCBI] 9.94791e-06
TCOF1 [NCBI] 9.66138e-06
EYA1 [NCBI] 9.08986e-06
PAX2 [NCBI] 7.97847e-06
SHOX [NCBI] 7.93673e-06
FGF3 [NCBI] 7.92304e-06
PAX8 [NCBI] 7.86936e-06
GDNF [NCBI] 6.28068e-06
MECP2 [NCBI] 5.83321e-06
TP63 [NCBI] 5.81741e-06
TNFRSF11A [NCBI] 5.10271e-06
TNFSF11 [NCBI] 4.86707e-06
PTH [NCBI] 2.17774e-06




OMIM


OMIM Link Information
gain
01
microtia with meatal atresia and conductive deafness [NCBI] 0.00306599
johnson neuroectodermal syndrome [NCBI] 0.00156207
microtia-anotia [NCBI] 0.00146918
OTSC4 [NCBI] 0.000993831
atresia of external auditory canal and conduction deafness [NCBI] 0.000776146
branchiootic syndrome 2 [NCBI] 0.000694153
earlobes, thickened, with conductive deafness from incudostapedial abnormalities [NCBI] 0.000694153
OSCS [NCBI] 0.000570168
klippel-feil syndrome, autosomal dominant [NCBI] 0.000521852
OTSC1 [NCBI] 0.000469717
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.000431005
varadi-papp syndrome [NCBI] 0.00042004
EEC1 [NCBI] 0.000289233
stapes ankylosis with broad thumb and toes [NCBI] 0.000199048
HFM [NCBI] 0.000170403
osteogenesis imperfecta, type i [NCBI] 0.000156776
SYNS1 [NCBI] 0.000153596
SYM1 [NCBI] 0.000151004
NOG [NCBI] 0.000132035
ossicular malformations, familial [NCBI] 0.00012182
deafness, conductive stapedial, with ear malformation and facial palsy [NCBI] 0.00012182
phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia [NCBI] 9.93556e-05
pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies [NCBI] 9.93556e-05
mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia [NCBI] 9.93556e-05
epiphyseal dysplasia, multiple, with myopia and conductive deafness [NCBI] 9.93556e-05
FOP [NCBI] 9.38487e-05
branchial arch syndrome, x-linked [NCBI] 8.53826e-05
gombo syndrome [NCBI] 8.53826e-05
zunich neuroectodermal syndrome [NCBI] 7.80401e-05
DFNA1 [NCBI] 7.53344e-05
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus [NCBI] 6.92003e-05
wildervanck syndrome [NCBI] 6.61183e-05
POU3F4 [NCBI] 6.58157e-05
OPD1 [NCBI] 6.2385e-05
LRS1 [NCBI] 6.13123e-05
EYA1 [NCBI] 5.81716e-05
SOST [NCBI] 5.76247e-05
CMDD [NCBI] 5.68226e-05
MNS [NCBI] 5.53307e-05
SLE [NCBI] 5.49151e-05
BWS [NCBI] 5.0311e-05
BOR1 [NCBI] 4.99544e-05
pfeiffer syndrome [NCBI] 4.94565e-05
DA2A [NCBI] 4.85058e-05
COL2A1 [NCBI] 4.5107e-05
FDH [NCBI] 4.4467e-05
down syndrome [NCBI] 4.31066e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 4.24691e-05
MECP2 [NCBI] 3.99763e-05
TCOF [NCBI] 3.81473e-05
GJB2 [NCBI] 3.77812e-05
AMC [NCBI] 3.76845e-05
velocardiofacial syndrome [NCBI] 3.74583e-05
CCD [NCBI] 3.44216e-05
PCD [NCBI] 2.38817e-05
CF [NCBI] 2.13417e-05
PTH [NCBI] 7.9829e-06
RA [NCBI] 3.94249e-06




Database Center for Life Science