Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Auditory Perception [NCBI]


Gene


Gene Link Information
Gain
01




OMIM


OMIM Link Information
gain
01
tune deafness [NCBI] 0.00110387
auditory neuropathy, autosomal dominant, 1 [NCBI] 0.00110387
auditory neuropathy, x-linked, 1, with peripheral sensory neuropathy [NCBI] 0.00110387
mohr syndrome [NCBI] 0.000869022
varadi-papp syndrome [NCBI] 0.000847798
JBTS1 [NCBI] 0.000710915
alport syndrome, autosomal dominant [NCBI] 0.000701422
musical perfect pitch [NCBI] 0.000198192
wildervanck syndrome [NCBI] 0.000120396
DFNA20 [NCBI] 0.000116365
USH1D [NCBI] 0.000105413
indifference to pain, congenital, autosomal recessive [NCBI] 9.99223e-05
DYX2 [NCBI] 9.43734e-05
DYX1 [NCBI] 8.56852e-05
LKS [NCBI] 7.69714e-05
CMT1B [NCBI] 7.37298e-05
PAX6 [NCBI] 6.18627e-05
ADHD [NCBI] 5.88942e-05
SCZD [NCBI] 5.84993e-05
PMD [NCBI] 5.29393e-05
BSN [NCBI] 4.22001e-05
CHRNA7 [NCBI] 3.89443e-05
AT [NCBI] 3.73996e-05
ACTG1 [NCBI] 3.68536e-05
HSR [NCBI] 3.33104e-05
CDH23 [NCBI] 3.33104e-05
TS [NCBI] 3.11627e-05
BDNF [NCBI] 1.95742e-05
AR [NCBI] 6.42093e-06
CCK [NCBI] 5.66627e-06
EPO [NCBI] 5.5338e-06
AVP [NCBI] 4.99082e-06
NPY [NCBI] 3.97909e-06




Database Center for Life Science