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Hippel-Lindau disease - translation to russian
A RARE GENETIC DISORDER CHARACTERIZED BY VISCERAL CYSTS AND BENIGN TUMORS IN MULTIPLE ORGAN SYSTEMS WITH POTENTIAL FOR SUBSEQUENT MALIGNANT CHANGE.
Von Hippel-Lindau Disease; Von Hippel-Lindau syndrome; VHL syndrome; VHL disease; Hippel-lindau disease; Cerebelloretinal Angiomatosis, familial; Angiomatosis retinae; Von Hippel-Lindau; Von Hippel Lindau; Von Hippel Lindau syndrome; Vhld; Von Hippel–Lindau syndrome; Von Hippel-Lindau disease; Von Hippel – Lindau syndrome; Angiomatosis retinate; Lindau-von Hippel disease; Lindau’s disease; Lindau's disease; Von Hippel-Lindau's disease; Von Hippel – Lindau disease; Von Hippel - Lindau syndrome; Von Hippel - Lindau disease; Von Hippel–Lindau Disease; Von Hippel–Lindau
![[[Slit lamp]] photograph showing [[retinal detachment]] in Von Hippel–Lindau disease](https://commons.wikimedia.org/wiki/Special:FilePath/Retinal detachment in Von Hippel-Lindau disease.jpg?width=200 "[[Slit lamp]] photograph showing [[retinal detachment]] in Von Hippel–Lindau disease")
von Hippel-Lindau disease
медицина
болезнь Гиппеля-Линдау
Hippel-Lindau disease
медицина
ангиофакоматоз
Bright's disease
![](https://commons.wikimedia.org/wiki/Special:FilePath/Richard Bright, "Reports of medical cases" Wellcome L0013468.jpg?width=200)
HISTORICAL CLASSIFICATION OF NEPHRITIS
Bright's Disease; Brights Disease; Blight's Disease; Bright disease; Bright's (renal) disease
существительное
медицина
брайтова болезнь, хронический нефрит
Definition
Bright's disease
·- An affection of the kidneys, usually inflammatory in character, and distinguished by the occurrence of albumin and renal casts in the urine. Several varieties of Bright's disease are now recognized, differing in the part of the kidney involved, and in the intensity and course of the morbid process.
Wikipedia
Von Hippel–Lindau disease
Von Hippel–Lindau disease (VHL), also known as Von Hippel–Lindau syndrome, is a rare genetic disorder with multisystem involvement. It is characterized by visceral cysts and benign tumors with potential for subsequent malignant transformation. It is a type of phakomatosis that results from a mutation in the Von Hippel–Lindau tumor suppressor gene on chromosome 3p25.3.
