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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM03862SALL2embryoMESH:D001862Bone Resorption
HM03862SALL2embryoMESH:D011297Prenatal Exposure Delayed Effects
HM03862SALL2embryoMESH:D014591Uterine Diseasesuterus
HM03862SALL2embryoMESH:D014591Uterine Diseasesplacenta
HM03862SALL2embryoMESH:D014591Uterine Diseasescervix
HM03862SALL2embryoMESH:D015451Leukemia, Lymphocytic, Chronic, B-Cellbone marrow
HM03862SALL2embryoMESH:D001943Breast Neoplasmsbreast
HM03862SALL2embryoMESH:D011471Prostatic Neoplasmsprostate
HM03862SALL2embryoMESH:D009421Nervous System Malformations
HM03862SALL2embryoMESH:D007333Insulin Resistance
HM03862SALL2embryoMESH:D010049Ovarian Diseasesovary
HM03862SALL2embryoMESH:D006331Heart Diseasesheart
HM03862SALL2embryoMESH:D019966Substance-Related Disorders
HM03862SALL2embryoMESH:D009369Neoplasmsspleen
HM03862SALL2embryoMESH:D009369Neoplasmsbone marrow
HM03862SALL2embryoMESH:D011629Puberty, Precocious
HM03862SALL2embryoMESH:D002278Carcinoma in Situ
HM03862SALL2embryoMESH:D002278Carcinoma in Situ