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MeSH keywords -> Related genes, diseases (OMIM)


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01 Vocal Cord Paralysis [NCBI]


Gene


Gene Link Information
Gain
01
CMT2C [NCBI] 0.000499621
GDAP1 [NCBI] 4.05927e-05
MUSK [NCBI] 2.15949e-05
NAIP [NCBI] 9.63071e-06
IGFBP1 [NCBI] 9.21259e-06
CNTF [NCBI] 7.85187e-06
BDNF [NCBI] 5.69162e-06
ACHE [NCBI] 5.57552e-06




OMIM


OMIM Link Information
gain
01
laryngeal abductor paralysis [NCBI] 0.00533174
HMN7A [NCBI] 0.0034825
hereditary motor and sensory neuropathy, type iic [NCBI] 0.0014884
LAP [NCBI] 0.0010375
MPD2 [NCBI] 0.000684465
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000473781
palatopharyngeal incompetence [NCBI] 0.000318072
laryngeal abductor paralysis [NCBI] 0.000272372
vocal cord paralysis and ptosis [NCBI] 0.00013578
laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy [NCBI] 0.00013578
GDNF [NCBI] 0.000134823
charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive [NCBI] 9.93282e-05
WBS [NCBI] 9.16538e-05
serpentine fibula-polycystic kidney syndrome [NCBI] 8.49166e-05
MJD [NCBI] 8.30369e-05
HNPP [NCBI] 5.49536e-05
RTS [NCBI] 5.46625e-05
AMC [NCBI] 5.12983e-05
CNTF [NCBI] 3.56463e-05
BDNF [NCBI] 2.36161e-05
ACHE [NCBI] 2.2459e-05
RA [NCBI] 2.0374e-05
SLE [NCBI] 1.80704e-05
PD [NCBI] 1.3374e-05
MG [NCBI] 6.17165e-06




Database Center for Life Science