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MeSH keywords -> Related genes, diseases (OMIM)


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01 Laurence-Moon Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
PIK3AP1 [NCBI] 1.93875e-05
MYO9A [NCBI] 1.93875e-05
OVOL1 [NCBI] 1.7007e-05
KIFC3 [NCBI] 1.7007e-05
ARL6 [NCBI] 1.5525e-05
RPS6KA4 [NCBI] 1.50912e-05
MKKS [NCBI] 1.19799e-05
TRPC6 [NCBI] 1.18594e-05
BBS1 [NCBI] 1.18022e-05
RCVRN [NCBI] 9.95474e-06
MEN1 [NCBI] 7.40511e-06
PRL [NCBI] 4.19396e-06



OMIM


 OMIM Link Information
gain		 01
BBS [NCBI] 0.00223207
laurence-moon syndrome [NCBI] 0.00022421
acrocephalopolysyndactyly type iii [NCBI] 0.000127341
tibia vara [NCBI] 0.000104875
retinitis pigmentosa, deafness, mental retardation, and hypogonadism [NCBI] 0.000104875
biemond syndrome ii [NCBI] 0.000104875
KIFC3 [NCBI] 0.000101216
fragile site 17p12 [NCBI] 9.08966e-05
MYO9A [NCBI] 8.7436e-05
carpenter syndrome [NCBI] 8.08408e-05
fragile site 2q11 [NCBI] 8.08408e-05
ARL6 [NCBI] 7.88574e-05
RP [NCBI] 7.50863e-05
TRPC6 [NCBI] 7.43448e-05
BBS4 [NCBI] 7.00104e-05
MKKS [NCBI] 5.59138e-05
KSS [NCBI] 3.05796e-05
fragile x mental retardation syndrome [NCBI] 2.94262e-05
PRL [NCBI] 1.36424e-05



Database Center for Life Science