DISEASES Urogenital Diseases [C12] Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications [C12.050] Female Urogenital Diseases and Pregnancy Complications Female Urogenital Diseases [C12.050.351] Female Urogenital Diseases Urologic Diseases [C12.050.351.968] Urologic Diseases Kidney Diseases [C12.050.351.968.419] Kidney Diseases Kidney Diseases, Cystic [C12.050.351.968.419.403] Kidney Diseases, Cystic Medullary Sponge Kidney [C12.050.351.968.419.403.500] Medullary Sponge Kidney Multicystic Dysplastic Kidney [C12.050.351.968.419.403.750] Multicystic Dysplastic Kidney Polycystic Kidney Diseases [C12.050.351.968.419.403.875] Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant [C12.050.351.968.419.403.875.500] Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive [C12.050.351.968.419.403.875.510] Polycystic Kidney, Autosomal Recessive DISEASES Urogenital Diseases [C12] Urogenital Diseases Male Urogenital Diseases [C12.200] Male Urogenital Diseases Urologic Diseases [C12.200.777] Urologic Diseases Kidney Diseases [C12.200.777.419] Kidney Diseases Kidney Diseases, Cystic [C12.200.777.419.403] Kidney Diseases, Cystic Medullary Sponge Kidney [C12.200.777.419.403.500] Medullary Sponge Kidney Multicystic Dysplastic Kidney [C12.200.777.419.403.750] Multicystic Dysplastic Kidney Polycystic Kidney Diseases [C12.200.777.419.403.875] Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant [C12.200.777.419.403.875.500] Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive [C12.200.777.419.403.875.510] Polycystic Kidney, Autosomal Recessive DISEASES Urogenital Diseases [C12] Urogenital Diseases Urologic Diseases [C12.950] Urologic Diseases Kidney Diseases [C12.950.419] Kidney Diseases Kidney Diseases, Cystic [C12.950.419.403] Kidney Diseases, Cystic Medullary Sponge Kidney [C12.950.419.403.500] Medullary Sponge Kidney Multicystic Dysplastic Kidney [C12.950.419.403.750] Multicystic Dysplastic Kidney Polycystic Kidney Diseases [C12.950.419.403.875] Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant [C12.950.419.403.875.500] Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive [C12.950.419.403.875.510] Polycystic Kidney, Autosomal Recessive DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormalities [C16.131] Congenital Abnormalities Abnormalities, Multiple [C16.131.077] Abnormalities, Multiple 22q11 Deletion Syndrome [C16.131.077.019] 22q11 Deletion Syndrome Alagille Syndrome [C16.131.077.065] Alagille Syndrome Angelman Syndrome [C16.131.077.095] Angelman Syndrome Barth Syndrome [C16.131.077.121] Barth Syndrome Basal Cell Nevus Syndrome [C16.131.077.130] Basal Cell Nevus Syndrome Beckwith-Wiedemann Syndrome [C16.131.077.133] Beckwith-Wiedemann Syndrome Bloom Syndrome [C16.131.077.137] Bloom Syndrome Branchio-Oto-Renal Syndrome [C16.131.077.208] Branchio-Oto-Renal Syndrome Carney Complex [C16.131.077.229] Carney Complex Ciliopathies [C16.131.077.245] Ciliopathies Cockayne Syndrome [C16.131.077.250] Cockayne Syndrome Costello Syndrome [C16.131.077.256] Costello Syndrome Cri-du-Chat Syndrome [C16.131.077.262] Cri-du-Chat Syndrome De Lange Syndrome [C16.131.077.272] De Lange Syndrome Deaf-Blind Disorders [C16.131.077.299] Deaf-Blind Disorders Donohue Syndrome [C16.131.077.313] Donohue Syndrome Down Syndrome [C16.131.077.327] Down Syndrome Ectodermal Dysplasia [C16.131.077.350] Ectodermal Dysplasia Fraser Syndrome [C16.131.077.371] Fraser Syndrome Gardner Syndrome [C16.131.077.393] Gardner Syndrome Heterotaxy Syndrome [C16.131.077.401] Heterotaxy Syndrome Holoprosencephaly [C16.131.077.410] Holoprosencephaly Incontinentia Pigmenti [C16.131.077.445] Incontinentia Pigmenti Isolated Noncompaction of the Ventricular Myocardium [C16.131.077.477] Isolated Noncompaction of the Ventricular Myocardium Laurence-Moon Syndrome [C16.131.077.509] Laurence-Moon Syndrome LEOPARD Syndrome [C16.131.077.525] LEOPARD Syndrome Loeys-Dietz Syndrome [C16.131.077.537] Loeys-Dietz Syndrome Marfan Syndrome [C16.131.077.550] Marfan Syndrome Mobius Syndrome [C16.131.077.578] Mobius Syndrome Monilethrix [C16.131.077.592] Monilethrix Nail-Patella Syndrome [C16.131.077.606] Nail-Patella Syndrome Netherton Syndrome [C16.131.077.619] Netherton Syndrome Nevus, Sebaceous of Jadassohn [C16.131.077.633] Nevus, Sebaceous of Jadassohn Oculocerebrorenal Syndrome [C16.131.077.662] Oculocerebrorenal Syndrome Orofaciodigital Syndromes [C16.131.077.676] Orofaciodigital Syndromes Pallister-Hall Syndrome [C16.131.077.690] Pallister-Hall Syndrome Pentalogy of Cantrell [C16.131.077.696] Pentalogy of Cantrell POEMS Syndrome [C16.131.077.703] POEMS Syndrome Polycystic Kidney Diseases [C16.131.077.717] Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant [C16.131.077.717.500] Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive [C16.131.077.717.510] Polycystic Kidney, Autosomal Recessive Prader-Willi Syndrome [C16.131.077.730] Prader-Willi Syndrome Prolidase Deficiency [C16.131.077.735] Prolidase Deficiency Proteus Syndrome [C16.131.077.740] Proteus Syndrome Prune Belly Syndrome [C16.131.077.745] Prune Belly Syndrome Rubella Syndrome, Congenital [C16.131.077.790] Rubella Syndrome, Congenital Rubinstein-Taybi Syndrome [C16.131.077.804] Rubinstein-Taybi Syndrome Short Rib-Polydactyly Syndrome [C16.131.077.850] Short Rib-Polydactyly Syndrome Silver-Russell Syndrome [C16.131.077.855] Silver-Russell Syndrome Smith-Lemli-Opitz Syndrome [C16.131.077.860] Smith-Lemli-Opitz Syndrome Smith-Magenis Syndrome [C16.131.077.879] Smith-Magenis Syndrome Sotos Syndrome [C16.131.077.889] Sotos Syndrome Trichothiodystrophy Syndromes [C16.131.077.899] Trichothiodystrophy Syndromes Trisomy 13 Syndrome [C16.131.077.919] Trisomy 13 Syndrome Trisomy 18 Syndrome [C16.131.077.929] Trisomy 18 Syndrome Waardenburg Syndrome [C16.131.077.938] Waardenburg Syndrome Weill-Marchesani Syndrome [C16.131.077.941] Weill-Marchesani Syndrome Wolf-Hirschhorn Syndrome [C16.131.077.944] Wolf-Hirschhorn Syndrome Zellweger Syndrome [C16.131.077.970] Zellweger Syndrome DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Genetic Diseases, Inborn [C16.320] Genetic Diseases, Inborn Ciliopathies [C16.320.184] Ciliopathies Alstrom Syndrome [C16.320.184.063] Alstrom Syndrome Bardet-Biedl Syndrome [C16.320.184.125] Bardet-Biedl Syndrome Caroli Disease [C16.320.184.250] Caroli Disease Ciliary Motility Disorders [C16.320.184.500] Ciliary Motility Disorders Polycystic Kidney Diseases [C16.320.184.625] Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant [C16.320.184.625.500] Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive [C16.320.184.625.510] Polycystic Kidney, Autosomal Recessive von Hippel-Lindau Disease [C16.320.184.750] von Hippel-Lindau Disease

Polycystic Kidney Diseases - Preferred

Concept UI	M0012031
Scope note	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.
Preferred term	Polycystic Kidney Diseases
Entry term(s)	Disease, Polycystic Kidney Disease, Polycystic Renal Diseases, Polycystic Kidney Diseases, Polycystic Renal Kidney Disease, Polycystic Kidney Diseases, Polycystic Polycystic Kidney Disease Polycystic Renal Disease Polycystic Renal Diseases Renal Disease, Polycystic Renal Diseases, Polycystic

Kidney, Polycystic - Related but not broader or narrower

Concept UI	M0482872
Preferred term	Kidney, Polycystic
Entry term(s)	Kidneys, Polycystic Polycystic Kidney Polycystic Kidneys