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Descriptor English: Polycystic Kidney, Autosomal Dominant
Descriptor Spanish: Riñón Poliquístico Autosómico Dominante
Descriptor riñón poliquístico autosómico dominante
Scope note: Trastornos renales con herencia autosómica dominante caracterizados por múltiples QUISTES en ambos RIÑONES con deterioro progresivo de la función renal.
Descriptor Portuguese: Rim Policístico Autossômico Dominante
Descriptor French: Polykystose rénale autosomique dominante
Entry term(s): ADPKD
Adult Polycystic Kidney Disease
Adult Polycystic Kidney Disease Type 1
Adult Polycystic Kidney Disease Type 2
Autosomal Dominant Polycystic Kidney
Kidney, Polycystic, Autosomal Dominant
Polycystic Kidney Disease 2
Polycystic Kidney Disease, Adult
Polycystic Kidney Disease, Adult Type 2
Polycystic Kidney Disease, Adult, Type II
Polycystic Kidney Disease, Autosomal Dominant
Polycystic Kidney Disease, Type 2
Polycystic Kidney, Type 1 Autosomal Dominant Disease
Polycystic Kidney, Type 2 Autosomal Dominant Disease
Tree number(s): C12.050.351.968.419.403.875.500
C12.200.777.419.403.875.500
C12.950.419.403.875.500
C16.131.077.717.500
C16.320.184.625.500
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D016891
Scope note: Kidney disorders with autosomal dominant inheritance and characterized by multiple CYSTS in both KIDNEYS with progressive deterioration of renal function.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Kidney, Polycystic (1974-1991)
Public MeSH Note: 1992; see KIDNEY, POLYCYSTIC, AUTOSOMAL DOMINANT 1992-2000
History Note: 1992
DeCS ID: 30024
Unique ID: D016891
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1992/01/01
Date of Entry: 1991/05/30
Revision Date: 2017/12/14
Polycystic Kidney, Autosomal Dominant - Preferred
Concept UI M0025702
Scope note Kidney disorders with autosomal dominant inheritance and characterized by multiple CYSTS in both KIDNEYS with progressive deterioration of renal function.
Preferred term Polycystic Kidney, Autosomal Dominant
Entry term(s) ADPKD
Adult Polycystic Kidney Disease
Autosomal Dominant Polycystic Kidney
Kidney, Polycystic, Autosomal Dominant
Polycystic Kidney Disease, Adult
Polycystic Kidney Disease, Autosomal Dominant
Polycystic Kidney, Type 2 Autosomal Dominant Disease - Narrower
Concept UI M0355417
Scope note Type 2 ADPKD is linked to gene mutation at the PKD2 locus on the long arm of CHROMOSOME 4.
Preferred term Polycystic Kidney, Type 2 Autosomal Dominant Disease
Entry term(s) Adult Polycystic Kidney Disease Type 2
Polycystic Kidney Disease 2
Polycystic Kidney Disease, Adult Type 2
Polycystic Kidney Disease, Adult, Type II
Polycystic Kidney Disease, Type 2
Polycystic Kidney, Type 1 Autosomal Dominant Disease - Narrower
Concept UI M0355414
Scope note Type 1 ADPKD is linked to gene mutation at the PKD1 locus on the short arm of CHROMOSOME 16.
Preferred term Polycystic Kidney, Type 1 Autosomal Dominant Disease
Entry term(s) Adult Polycystic Kidney Disease Type 1



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