NALT

Término preferido

autosomal recessive polycystic kidney disease

Topic

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.

polycystic kidney diseases

infantile polycystic kidney disease type I

Field 001 in MARC Authority Format

63642

español

enfermedad renal poliquística autosómica recesiva

URI

https://lod.nal.usda.gov/nalt/219148

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Creado 6/19/14, última modificación 11/17/17