Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Birth Order [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
trichoepithelioma, multiple familial [NCBI] 0.000833714
acetabular dysplasia [NCBI] 0.000801832
hodgkin disease, x-linked pseudoautosomal [NCBI] 0.000801832
OTSC1 [NCBI] 0.000710576
OFC1 [NCBI] 0.000409023
autism [NCBI] 0.000380133
hemochromatosis, neonatal [NCBI] 0.000223007
IHPS1 [NCBI] 0.000198634
IS1 [NCBI] 0.000198095
HMS1 [NCBI] 0.000188977
TD1 [NCBI] 0.000130402
LNPEP [NCBI] 9.95021e-05
corticosterone methyloxidase type i deficiency [NCBI] 9.90237e-05
kawasaki disease [NCBI] 8.6096e-05
CPI [NCBI] 8.5861e-05
tetralogy of fallot [NCBI] 8.10864e-05
cri-du-chat syndrome [NCBI] 8.10864e-05
hodgkin lymphoma [NCBI] 7.09344e-05
EFE [NCBI] 7.00725e-05
neural tube defects [NCBI] 6.69608e-05
apert syndrome [NCBI] 6.62546e-05
LGMD2C [NCBI] 6.49146e-05
FOP [NCBI] 5.9819e-05
osteogenesis imperfecta, type iia [NCBI] 5.66165e-05
RA [NCBI] 5.55631e-05
HD [NCBI] 4.4013e-05
VHL [NCBI] 4.18777e-05
lymphoma, non-hodgkin, familial [NCBI] 4.18245e-05
SCZD [NCBI] 4.16868e-05
FRDA [NCBI] 4.09428e-05
ACH [NCBI] 3.98811e-05
JARID1D [NCBI] 3.95298e-05
CYP11B2 [NCBI] 3.53128e-05
RTT [NCBI] 2.54594e-05
hemophilia a [NCBI] 2.51861e-05
NF1 [NCBI] 2.25607e-05
GTS [NCBI] 2.10249e-05
TS [NCBI] 1.61267e-05
CD [NCBI] 1.18916e-05
FA [NCBI] 1.1574e-05
CF [NCBI] 2.36594e-06
AD [NCBI] 7.39775e-09



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