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Autosomal recessive polycystic kidney disease. 2001

A Sessa, and M Meroni, and M Righetti, and G Battini, and A Maglio, and S L Puricelli
Unità Operativa di Nefrologia e Dialisi, Ospedale di Vimercate, Italia. adsess@tin.it

UI MeSH Term Description Entries
D011296 Prenatal Diagnosis Determination of the nature of a pathological condition or disease in the postimplantation EMBRYO; FETUS; or pregnant female before birth. Diagnosis, Prenatal,Fetal Diagnosis,Fetal Imaging,Fetal Screening,Intrauterine Diagnosis,Antenatal Diagnosis,Antenatal Screening,Diagnosis, Antenatal,Diagnosis, Intrauterine,Prenatal Screening,Antenatal Diagnoses,Antenatal Screenings,Diagnosis, Fetal,Fetal Diagnoses,Fetal Imagings,Fetal Screenings,Imaging, Fetal,Intrauterine Diagnoses,Prenatal Diagnoses,Prenatal Screenings,Screening, Antenatal,Screening, Fetal,Screening, Prenatal
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D017044 Polycystic Kidney, Autosomal Recessive A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY. Autosomal Recessive Polycystic Kidney,Autosomal Recessive Polycystic Kidney Disease,Kidney, Polycystic, Autosomal Recessive,Polycystic Kidney Disease, Infantile, Type I,ARPKD,Polycystic Kidney Disease, Autosomal Recessive,Polycystic Kidney Disease, Infantile, Type 1,Polycystic Kidney and Hepatic Disease 1,Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive)

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