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MeSH keywords -> Related genes, diseases (OMIM)


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01 Microstomia [NCBI]


Gene


Gene Link Information
Gain
01
HFM [NCBI] 0.0014682




OMIM


OMIM Link Information
gain
01
auriculocondylar syndrome [NCBI] 0.00282758
HFM [NCBI] 0.00278603
dysgnathia complex [NCBI] 0.000705355
DA2A [NCBI] 0.000626089
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.000605677
stuve-wiedemann syndrome [NCBI] 0.000193501
cranioacrofacial syndrome [NCBI] 0.000143802
kniest-like dysplasia with pursed lips and ectopia lentis [NCBI] 0.000121332
limb deficiencies, distal, with micrognathia [NCBI] 0.000121332
brachycephaly, deafness, cataract, microstomia, and mental retardation [NCBI] 0.000107346
PWS [NCBI] 2.33235e-05




Database Center for Life Science