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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM06199RNF38thyroidMESH:D002278Carcinoma in Situ
HM06199RNF38thyroidMESH:D002278Carcinoma in Situ
HM06199RNF38thyroidMESH:D001862Bone Resorption
HM06199RNF38thyroidMESH:D007249Inflammation
HM06199RNF38thyroidMESH:D009421Nervous System Malformations
HM06199RNF38thyroidMESH:D014591Uterine Diseasesuterus
HM06199RNF38thyroidMESH:D014591Uterine Diseasesplacenta
HM06199RNF38thyroidMESH:D014591Uterine Diseasescervix
HM06199RNF38thyroidMESH:D019966Substance-Related Disorders
HM06199RNF38thyroidMESH:D004938Esophageal Neoplasms
HM06199RNF38thyroidMESH:D011629Puberty, Precocious
HM06199RNF38thyroidMESH:D011297Prenatal Exposure Delayed Effects
HM06199RNF38thyroidMESH:D011471Prostatic Neoplasmsprostate
HM06199RNF38thyroidMESH:D001943Breast Neoplasmsbreast
HM06199RNF38thyroidMESH:D010049Ovarian Diseasesovary
HM06199RNF38thyroidMESH:D007333Insulin Resistance
HM06199RNF38thyroidMESH:D002471Cell Transformation, Neoplastic