Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Reflex, Pupillary [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.00029087
AKR1B1 [NCBI] 7.1981e-06
RPE65 [NCBI] 6.74738e-06
ACHE [NCBI] 6.34028e-06
LMX1A [NCBI] 3.943e-06
AKR1B10 [NCBI] 3.59619e-06
PHOX2A [NCBI] 3.4431e-06
CHRM1 [NCBI] 3.37112e-06
SIX3 [NCBI] 3.08838e-06
MPZ [NCBI] 3.05766e-06
CRH [NCBI] 2.62034e-06
PAX6 [NCBI] 2.12239e-06



OMIM


 OMIM Link Information
gain		 01
ophthalmoplegia, progressive, with scrotal tongue and mental deficiency [NCBI] 0.000176977
paralysis agitans, juvenile, of hunt [NCBI] 0.000149206
optic nerve hypoplasia, bilateral [NCBI] 0.000126861
charcot-marie-tooth disease, axonal, type 2j [NCBI] 0.00012283
DRD [NCBI] 9.46272e-05
gaucher disease, type iii [NCBI] 9.29264e-05
OPN4 [NCBI] 9.22514e-05
RP [NCBI] 8.7464e-05
leber optic atrophy [NCBI] 5.3567e-05
ACHE [NCBI] 4.4399e-05
CRY2 [NCBI] 3.70547e-05
CRY1 [NCBI] 3.5127e-05
PDE6B [NCBI] 3.39677e-05
MPZ [NCBI] 2.87249e-05
CRH [NCBI] 9.06921e-06
SLE [NCBI] 6.65995e-06
RA [NCBI] 3.10215e-06



Database Center for Life Science