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Polycystic Kidney Diseases
Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance.
推出的年份: 1991
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C12.050.351.968.419.403.875, C12.200.777.419.403.875, C12.950.419.403.875, C16.131.077.717, C16.320.184.625
MeSH 单一 ID:
D007690
进入的组:
Disease, Polycystic Kidney
Diseases, Polycystic Kidney
Kidney Disease, Polycystic
Kidney Diseases, Polycystic
Polycystic Kidney Disease
Polycystic Renal Disease
Disease, Polycystic Renal
Diseases, Polycystic Renal
Polycystic Renal Diseases
Renal Disease, Polycystic
Renal Diseases, Polycystic
Kidney, Polycystic
Polycystic Kidneys
Polycystic Kidney
Kidneys, Polycystic
All MeSH Categories
Diseases Category
Urogenital Diseases [C12]
Female Urogenital Diseases and Pregnancy Complications [C12.050]
Female Urogenital Diseases [C12.050.351]
Urologic Diseases [C12.050.351.968]
Kidney Diseases [C12.050.351.968.419]
Kidney Diseases, Cystic [C12.050.351.968.419.403]
Medullary Sponge Kidney [C12.050.351.968.419.403.500]
Multicystic Dysplastic Kidney [C12.050.351.968.419.403.750]
Polycystic Kidney Diseases [C12.050.351.968.419.403.875]
Polycystic Kidney, Autosomal Dominant [C12.050.351.968.419.403.875.500]
Polycystic Kidney, Autosomal Recessive [C12.050.351.968.419.403.875.510]
All MeSH Categories
Diseases Category
Urogenital Diseases [C12]
Male Urogenital Diseases [C12.200]
Urologic Diseases [C12.200.777]
Kidney Diseases [C12.200.777.419]
Kidney Diseases, Cystic [C12.200.777.419.403]
Medullary Sponge Kidney [C12.200.777.419.403.500]
Multicystic Dysplastic Kidney [C12.200.777.419.403.750]
Polycystic Kidney Diseases [C12.200.777.419.403.875]
Polycystic Kidney, Autosomal Dominant [C12.200.777.419.403.875.500]
Polycystic Kidney, Autosomal Recessive [C12.200.777.419.403.875.510]
All MeSH Categories
Diseases Category
Urogenital Diseases [C12]
Urologic Diseases [C12.950]
Kidney Diseases [C12.950.419]
Kidney Diseases, Cystic [C12.950.419.403]
Medullary Sponge Kidney [C12.950.419.403.500]
Multicystic Dysplastic Kidney [C12.950.419.403.750]
Polycystic Kidney Diseases [C12.950.419.403.875]
Polycystic Kidney, Autosomal Dominant [C12.950.419.403.875.500]
Polycystic Kidney, Autosomal Recessive [C12.950.419.403.875.510]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
22q11 Deletion Syndrome [C16.131.077.019]
add_circle
Alagille Syndrome [C16.131.077.065]
Angelman Syndrome [C16.131.077.095]
Barth Syndrome [C16.131.077.121]
Basal Cell Nevus Syndrome [C16.131.077.130]
Beckwith-Wiedemann Syndrome [C16.131.077.133]
Bloom Syndrome [C16.131.077.137]
Branchio-Oto-Renal Syndrome [C16.131.077.208]
Carney Complex [C16.131.077.229]
CHARGE Syndrome [C16.131.077.239]
Ciliopathies [C16.131.077.245]
add_circle
Cockayne Syndrome [C16.131.077.250]
Costello Syndrome [C16.131.077.256]
Cri-du-Chat Syndrome [C16.131.077.262]
De Lange Syndrome [C16.131.077.272]
Deaf-Blind Disorders [C16.131.077.299]
add_circle
Donohue Syndrome [C16.131.077.313]
Down Syndrome [C16.131.077.327]
Ectodermal Dysplasia [C16.131.077.350]
add_circle
Fraser Syndrome [C16.131.077.371]
Gardner Syndrome [C16.131.077.393]
Heterotaxy Syndrome [C16.131.077.401]
Holoprosencephaly [C16.131.077.410]
Incontinentia Pigmenti [C16.131.077.445]
Isolated Noncompaction of the Ventricular Myocardium [C16.131.077.477]
Laurence-Moon Syndrome [C16.131.077.509]
LEOPARD Syndrome [C16.131.077.525]
Loeys-Dietz Syndrome [C16.131.077.537]
Marfan Syndrome [C16.131.077.550]
Mobius Syndrome [C16.131.077.578]
Monilethrix [C16.131.077.592]
Nail-Patella Syndrome [C16.131.077.606]
Netherton Syndrome [C16.131.077.619]
Nevus, Sebaceous of Jadassohn [C16.131.077.633]
Oculocerebrorenal Syndrome [C16.131.077.662]
Orofaciodigital Syndromes [C16.131.077.676]
Pallister-Hall Syndrome [C16.131.077.690]
Pentalogy of Cantrell [C16.131.077.696]
POEMS Syndrome [C16.131.077.703]
Polycystic Kidney Diseases [C16.131.077.717]
Polycystic Kidney, Autosomal Dominant [C16.131.077.717.500]
Polycystic Kidney, Autosomal Recessive [C16.131.077.717.510]
Prader-Willi Syndrome [C16.131.077.730]
Prolidase Deficiency [C16.131.077.735]
Proteus Syndrome [C16.131.077.740]
Prune Belly Syndrome [C16.131.077.745]
Rubella Syndrome, Congenital [C16.131.077.790]
Rubinstein-Taybi Syndrome [C16.131.077.804]
Short Rib-Polydactyly Syndrome [C16.131.077.850]
Silver-Russell Syndrome [C16.131.077.855]
Smith-Lemli-Opitz Syndrome [C16.131.077.860]
Smith-Magenis Syndrome [C16.131.077.879]
Sotos Syndrome [C16.131.077.889]
Trichothiodystrophy Syndromes [C16.131.077.899]
Trisomy 13 Syndrome [C16.131.077.919]
Trisomy 18 Syndrome [C16.131.077.929]
Waardenburg Syndrome [C16.131.077.938]
Weill-Marchesani Syndrome [C16.131.077.941]
Wolf-Hirschhorn Syndrome [C16.131.077.944]
Zellweger Syndrome [C16.131.077.970]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Ciliopathies [C16.320.184]
Alstrom Syndrome [C16.320.184.063]
Bardet-Biedl Syndrome [C16.320.184.125]
Caroli Disease [C16.320.184.250]
Ciliary Motility Disorders [C16.320.184.500]
add_circle
Polycystic Kidney Diseases [C16.320.184.625]
Polycystic Kidney, Autosomal Dominant [C16.320.184.625.500]
Polycystic Kidney, Autosomal Recessive [C16.320.184.625.510]
von Hippel-Lindau Disease [C16.320.184.750]
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