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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM04675CABP4eyeMESH:D001862Bone Resorption
HM04675CABP4eyeMESH:D014591Uterine Diseasesuterus
HM04675CABP4eyeMESH:D014591Uterine Diseasesplacenta
HM04675CABP4eyeMESH:D014591Uterine Diseasescervix
HM04675CABP4eyeMESH:D002278Carcinoma in Situ
HM04675CABP4eyeMESH:D002278Carcinoma in Situ
HM04675CABP4eyeMESH:D011297Prenatal Exposure Delayed Effects
HM04675CABP4eyeMESH:D019966Substance-Related Disorders
HM04675CABP4eyeMESH:D011629Puberty, Precocious
HM04675CABP4eyeMESH:D011471Prostatic Neoplasmsprostate
HM04675CABP4eyeMESH:D000860Anoxia
HM04675CABP4eyeMESH:D007333Insulin Resistance
HM04675CABP4eyeOMIM:610427NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B
HM04675CABP4eyeMESH:D006527Hepatolenticular Degenerationliver
HM04675CABP4eyeMESH:D007022Hypotension
HM04675CABP4eyeMESH:D000138Acidosis
HM04675CABP4eyeMESH:D001943Breast Neoplasmsbreast
HM04675CABP4eyeMESH:D010049Ovarian Diseasesovary
HM04675CABP4eyeMESH:D009421Nervous System Malformations