Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Sex Chromosome Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
ARX [NCBI] 3.65652e-05
SLC6A8 [NCBI] 2.62229e-05
MID2 [NCBI] 1.40261e-05
PHF6 [NCBI] 1.33737e-05
SOX1 [NCBI] 1.32017e-05
BMP15 [NCBI] 1.16119e-05
XK [NCBI] 1.1487e-05
SLC16A2 [NCBI] 1.13705e-05
GDF9 [NCBI] 1.12615e-05
USP9Y [NCBI] 1.08838e-05
L1CAM [NCBI] 1.02237e-05
SHOX [NCBI] 8.95762e-06
SRY [NCBI] 8.18462e-06
MECP2 [NCBI] 6.84729e-06
FMR1 [NCBI] 5.75274e-06
JAK2 [NCBI] 5.63602e-06



OMIM


 OMIM Link Information
gain		 01
PCD [NCBI] 0.000907885
BFLS [NCBI] 0.000201129
corpus callosum, agenesis of, with abnormal genitalia [NCBI] 0.00012962
ARX [NCBI] 0.000128432
LISX2 [NCBI] 0.000111537
MRX54 [NCBI] 0.000111537
SRY [NCBI] 0.000111394
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [NCBI] 0.000105561
creatine deficiency syndrome, x-linked [NCBI] 0.000103239
RP3 [NCBI] 8.05159e-05
PHF6 [NCBI] 7.46818e-05
SLC6A8 [NCBI] 6.3036e-05
L1CAM [NCBI] 5.35982e-05
CF [NCBI] 2.32532e-06



Database Center for Life Science