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MeSH keywords -> Related genes, diseases (OMIM)


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01 Retinal Dysplasia [NCBI]

Gene


 Gene Link Information
Gain		 01
PRD [NCBI] 0.000438875
CTD [NCBI] 0.000378131
NDP [NCBI] 5.22359e-05
ABCG4 [NCBI] 1.47454e-05
MFRP [NCBI] 1.32017e-05
CRX [NCBI] 1.20435e-05
NR2E3 [NCBI] 1.20435e-05
RP1 [NCBI] 1.11927e-05
PDE6B [NCBI] 1.10417e-05
FKTN [NCBI] 1.04903e-05
PAX6 [NCBI] 7.88489e-06



OMIM


 OMIM Link Information
gain		 01
lymphedema, microcephaly, chorioretinopathy syndrome [NCBI] 0.00368744
RNANC [NCBI] 0.00074746
ND [NCBI] 0.000257318
chorioretinal dysplasia-microcephaly-mental retardation syndrome [NCBI] 0.000240246
NDP [NCBI] 0.000132171
PRD [NCBI] 0.000113601
coats disease [NCBI] 0.000109506
RP [NCBI] 8.16166e-05
NR2E3 [NCBI] 7.46818e-05
PTCH1 [NCBI] 6.27854e-05
PDE6B [NCBI] 5.89909e-05



Database Center for Life Science