GB83Ангилал

Nephronophthisis

Тодорхойлолт

Autosomal recessive disease characterised by polyuria, polydipsia, enuresis and chronic kidney disease with end stage renal failure occurring between birth and late adolescence depending on the NPHP gene involved. Extra-renal manifestations occur with associated multisystem genetic disorders (e.g. Senior-Loken, Cogan, Joubert)

Индексийн нэр томьёо Index terms · 3

NephronophthisisAdult familial nephronophthisis - spastic quadriparesiaJuvenile nephronophthisis

Монгол орчуулга хянагдаж байгаа тул англи эхийг харуулж байна. Эх сурвалж: WHO ICD-11 (MMS) · WHO сайтад харах ↗